InvaGen Pharmaceuticals Inc
FDA Approved Drugs

InvaGen Pharmaceuticals Inc

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX Discontinued Unclassified
  • Total Records 170
  • Latest Approval Date Feb 20, 2026
  • Data Source FDA
  • First Approval Date Apr 20, 2005
All
170
View
Unclassified
2
View
Discontinued
63
View
RX
105
View
Company Overview

Company

InvaGen Pharmaceuticals Inc

Country

U.S.A

Website

Visit Website

Email

Social Profiles

Company Snapshot

InvaGen Pharmaceuticals Inc

7 Oser Avenue ,Hauppauge, NY 11788

U.S.A

www.invagen.com/ View on Map
FDA Approved Drug Records ( 170 records )
2012
17 Jan
RX Application: 90284

Drug Name

ALFUZOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2012-01-17

90284 / 1

Active Ingredient

ALFUZOSIN HYDROCHLORIDE

Application Number

90284

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2012-01-17

Regulatory Status

RX

2016
30 Sep
Discontinued Application: 207570

Drug Name

AMANTADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2016-09-30

207570 / 1

Active Ingredient

AMANTADINE HYDROCHLORIDE

Application Number

207570

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2016-09-30

Regulatory Status

Discontinued

2017
31 Jan
Discontinued Application: 207571

Drug Name

AMANTADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2017-01-31

207571 / 1

Active Ingredient

AMANTADINE HYDROCHLORIDE

Application Number

207571

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2017-01-31

Regulatory Status

Discontinued

2007
28 Aug
RX Application: 77955

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-08-28

77955 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77955

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-08-28

Regulatory Status

RX

2007
28 Aug
RX Application: 77955

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-08-28

77955 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77955

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-08-28

Regulatory Status

RX

2007
28 Aug
RX Application: 77955

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-08-28

77955 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77955

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-08-28

Regulatory Status

RX

2015
10 Dec
RX Application: 206367

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2015-12-10

206367 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

206367

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2015-12-10

Regulatory Status

RX

2015
10 Dec
RX Application: 206367

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-12-10

206367 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

206367

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2015-12-10

Regulatory Status

RX

2015
10 Dec
RX Application: 206367

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-12-10

206367 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

206367

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-12-10

Regulatory Status

RX

2017
09 Jan
Discontinued Application: 204846

Drug Name

ATORVASTATIN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2017-01-09

204846 / 1

Active Ingredient

ATORVASTATIN CALCIUM

Application Number

204846

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 204846

Drug Name

ATORVASTATIN CALCIUM

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2017-01-09

204846 / 2

Active Ingredient

ATORVASTATIN CALCIUM

Application Number

204846

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 204846

Drug Name

ATORVASTATIN CALCIUM

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2017-01-09

204846 / 3

Active Ingredient

ATORVASTATIN CALCIUM

Application Number

204846

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2017-01-09

Regulatory Status

Discontinued

2017
09 Jan
Discontinued Application: 204846

Drug Name

ATORVASTATIN CALCIUM

Product Number

4

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2017-01-09

204846 / 4

Active Ingredient

ATORVASTATIN CALCIUM

Application Number

204846

Product Number

4

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2017-01-09

Regulatory Status

Discontinued

2010
29 Mar
Discontinued Application: 90294

Drug Name

BENZTROPINE MESYLATE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2010-03-29

90294 / 1

Active Ingredient

BENZTROPINE MESYLATE

Application Number

90294

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2010-03-29

Regulatory Status

Discontinued

2010
29 Mar
Discontinued Application: 90294

Drug Name

BENZTROPINE MESYLATE

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2010-03-29

90294 / 2

Active Ingredient

BENZTROPINE MESYLATE

Application Number

90294

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2010-03-29

Regulatory Status

Discontinued

2010
29 Mar
Discontinued Application: 90294

Drug Name

BENZTROPINE MESYLATE

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2010-03-29

90294 / 3

Active Ingredient

BENZTROPINE MESYLATE

Application Number

90294

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2010-03-29

Regulatory Status

Discontinued

2016
26 Aug
Discontinued Application: 206556

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2016-08-26

206556 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

206556

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2016-08-26

Regulatory Status

Discontinued

2016
26 Aug
Discontinued Application: 206556

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2016-08-26

206556 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

206556

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2016-08-26

Regulatory Status

Discontinued

2016
09 Feb
Discontinued Application: 206674

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2016-02-09

206674 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

206674

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2016-02-09

Regulatory Status

Discontinued

2016
09 Feb
Discontinued Application: 206674

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2016-02-09

206674 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

206674

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2016-02-09

Regulatory Status

Discontinued

2016
09 Feb
Discontinued Application: 206674

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2016-02-09

206674 / 3

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

206674

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2016-02-09

Regulatory Status

Discontinued

2017
18 Sep
Discontinued Application: 207389

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2017-09-18

207389 / 1

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

207389

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2017-09-18

Regulatory Status

Discontinued

2017
18 Sep
Discontinued Application: 207389

Drug Name

BUPROPION HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-09-18

207389 / 2

Active Ingredient

BUPROPION HYDROCHLORIDE

Application Number

207389

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2017-09-18

Regulatory Status

Discontinued

2013
07 Feb
RX Application: 203135

Drug Name

CALCIUM ACETATE

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2013-02-07

203135 / 1

Active Ingredient

CALCIUM ACETATE

Application Number

203135

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2013-02-07

Regulatory Status

RX

2006
03 Oct
RX Application: 77534

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-10-03

77534 / 1

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77534

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-10-03

Regulatory Status

RX

2006
03 Oct
RX Application: 77534

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-10-03

77534 / 2

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77534

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-10-03

Regulatory Status

RX

2006
03 Oct
RX Application: 77534

Drug Name

CITALOPRAM HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-10-03

77534 / 3

Active Ingredient

CITALOPRAM HYDROBROMIDE

Application Number

77534

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-10-03

Regulatory Status

RX

2020
20 Apr
Discontinued Application: 212602

Drug Name

COLESEVELAM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

625MG

Approval Date

2020-04-20

212602 / 1

Active Ingredient

COLESEVELAM HYDROCHLORIDE

Application Number

212602

Product Number

1

Dosage Form

-

Strength

625MG

Approval Date

2020-04-20

Regulatory Status

Discontinued

2010
23 Jul
RX Application: 90478

Drug Name

CYCLOBENZAPRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-07-23

90478 / 1

Active Ingredient

CYCLOBENZAPRINE HYDROCHLORIDE

Application Number

90478

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-07-23

Regulatory Status

RX

2010
23 Jul
RX Application: 90478

Drug Name

CYCLOBENZAPRINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2010-07-23

90478 / 2

Active Ingredient

CYCLOBENZAPRINE HYDROCHLORIDE

Application Number

90478

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2010-07-23

Regulatory Status

RX

2012
11 Sep
RX Application: 78604

Drug Name

ESCITALOPRAM OXALATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-09-11

78604 / 1

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

78604

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-09-11

Regulatory Status

RX

2012
11 Sep
RX Application: 78604

Drug Name

ESCITALOPRAM OXALATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-09-11

78604 / 2

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

78604

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-09-11

Regulatory Status

RX

2012
11 Sep
RX Application: 78604

Drug Name

ESCITALOPRAM OXALATE

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2012-09-11

78604 / 3

Active Ingredient

ESCITALOPRAM OXALATE

Application Number

78604

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2012-09-11

Regulatory Status

RX

2017
28 Mar
Discontinued Application: 207378

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

1

Dosage Form

-

Strength

67MG

Approval Date

2017-03-28

207378 / 1

Active Ingredient

FENOFIBRATE

Application Number

207378

Product Number

1

Dosage Form

-

Strength

67MG

Approval Date

2017-03-28

Regulatory Status

Discontinued

2017
28 Mar
Discontinued Application: 207378

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

2

Dosage Form

-

Strength

134MG

Approval Date

2017-03-28

207378 / 2

Active Ingredient

FENOFIBRATE

Application Number

207378

Product Number

2

Dosage Form

-

Strength

134MG

Approval Date

2017-03-28

Regulatory Status

Discontinued

2017
28 Mar
Discontinued Application: 207378

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-03-28

207378 / 3

Active Ingredient

FENOFIBRATE

Application Number

207378

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-03-28

Regulatory Status

Discontinued

2005
20 Apr
RX Application: 77222

Drug Name

FOSINOPRIL SODIUM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-04-20

77222 / 1

Active Ingredient

FOSINOPRIL SODIUM

Application Number

77222

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-04-20

Regulatory Status

RX

2005
20 Apr
RX Application: 77222

Drug Name

FOSINOPRIL SODIUM

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2005-04-20

77222 / 2

Active Ingredient

FOSINOPRIL SODIUM

Application Number

77222

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2005-04-20

Regulatory Status

RX

2005
20 Apr
RX Application: 77222

Drug Name

FOSINOPRIL SODIUM

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2005-04-20

77222 / 3

Active Ingredient

FOSINOPRIL SODIUM

Application Number

77222

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2005-04-20

Regulatory Status

RX

2009
09 Jul
RX Application: 90228

Drug Name

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

2009-07-09

90228 / 1

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

90228

Product Number

1

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

2009-07-09

Regulatory Status

RX

2009
09 Jul
RX Application: 90228

Drug Name

FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

2009-07-09

90228 / 2

Active Ingredient

FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

Application Number

90228

Product Number

2

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

2009-07-09

Regulatory Status

RX

2009
30 Dec
RX Application: 90705

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2009-12-30

90705 / 1

Active Ingredient

GABAPENTIN

Application Number

90705

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2009-12-30

Regulatory Status

RX

2009
30 Dec
RX Application: 90705

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2009-12-30

90705 / 2

Active Ingredient

GABAPENTIN

Application Number

90705

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2009-12-30

Regulatory Status

RX

2009
30 Dec
RX Application: 90705

Drug Name

GABAPENTIN

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2009-12-30

90705 / 3

Active Ingredient

GABAPENTIN

Application Number

90705

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2009-12-30

Regulatory Status

RX

2012
16 Oct
Discontinued Application: 202764

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2012-10-16

202764 / 1

Active Ingredient

GABAPENTIN

Application Number

202764

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2012-10-16

Regulatory Status

Discontinued

2012
16 Oct
Discontinued Application: 202764

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2012-10-16

202764 / 2

Active Ingredient

GABAPENTIN

Application Number

202764

Product Number

2

Dosage Form

-

Strength

800MG

Approval Date

2012-10-16

Regulatory Status

Discontinued

2006
27 Jul
RX Application: 77836

Drug Name

GEMFIBROZIL

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2006-07-27

77836 / 1

Active Ingredient

GEMFIBROZIL

Application Number

77836

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2006-07-27

Regulatory Status

RX

2008
15 Dec
Discontinued Application: 90255

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2008-12-15

90255 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

90255

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2008-12-15

Regulatory Status

Discontinued

2008
15 Dec
Discontinued Application: 90255

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2008-12-15

90255 / 2

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

90255

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2008-12-15

Regulatory Status

Discontinued

2008
15 Dec
Discontinued Application: 90255

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2008-12-15

90255 / 3

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

90255

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2008-12-15

Regulatory Status

Discontinued

2008
15 Dec
Discontinued Application: 90255

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2008-12-15

90255 / 4

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

90255

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2008-12-15

Regulatory Status

Discontinued

-
Unclassified Application: 78850

Drug Name

LAMIVUDINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

78850 / 1

Active Ingredient

LAMIVUDINE

Application Number

78850

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 78850

Drug Name

LAMIVUDINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

78850 / 2

Active Ingredient

LAMIVUDINE

Application Number

78850

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

2021
17 Dec
RX Application: 215395

Drug Name

LANREOTIDE ACETATE

Product Number

1

Dosage Form

-

Strength

EQ 60MG BASE/0.2ML (EQ 60MG BASE/0.2ML)

Approval Date

2021-12-17

215395 / 1

Active Ingredient

LANREOTIDE ACETATE

Application Number

215395

Product Number

1

Dosage Form

-

Strength

EQ 60MG BASE/0.2ML (EQ 60MG BASE/0.2ML)

Approval Date

2021-12-17

Regulatory Status

RX

2021
17 Dec
RX Application: 215395

Drug Name

LANREOTIDE ACETATE

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE/0.3ML (EQ 90MG BASE/0.3ML)

Approval Date

2021-12-17

215395 / 2

Active Ingredient

LANREOTIDE ACETATE

Application Number

215395

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE/0.3ML (EQ 90MG BASE/0.3ML)

Approval Date

2021-12-17

Regulatory Status

RX

2021
17 Dec
RX Application: 215395

Drug Name

LANREOTIDE ACETATE

Product Number

3

Dosage Form

-

Strength

EQ 120MG BASE/0.5ML (EQ 120MG BASE/0.5ML)

Approval Date

2021-12-17

215395 / 3

Active Ingredient

LANREOTIDE ACETATE

Application Number

215395

Product Number

3

Dosage Form

-

Strength

EQ 120MG BASE/0.5ML (EQ 120MG BASE/0.5ML)

Approval Date

2021-12-17

Regulatory Status

RX

2024
21 May
RX Application: 217193

Drug Name

LANREOTIDE ACETATE

Product Number

1

Dosage Form

-

Strength

EQ 60MG BASE/0.2ML (EQ 60MG BASE/0.2ML)

Approval Date

2024-05-21

217193 / 1

Active Ingredient

LANREOTIDE ACETATE

Application Number

217193

Product Number

1

Dosage Form

-

Strength

EQ 60MG BASE/0.2ML (EQ 60MG BASE/0.2ML)

Approval Date

2024-05-21

Regulatory Status

RX

2024
21 May
RX Application: 217193

Drug Name

LANREOTIDE ACETATE

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE/0.3ML (EQ 90MG BASE/0.3ML)

Approval Date

2024-05-21

217193 / 2

Active Ingredient

LANREOTIDE ACETATE

Application Number

217193

Product Number

2

Dosage Form

-

Strength

EQ 90MG BASE/0.3ML (EQ 90MG BASE/0.3ML)

Approval Date

2024-05-21

Regulatory Status

RX

2024
21 May
RX Application: 217193

Drug Name

LANREOTIDE ACETATE

Product Number

3

Dosage Form

-

Strength

EQ 120MG BASE/0.5ML (EQ 120MG BASE/0.5ML)

Approval Date

2024-05-21

217193 / 3

Active Ingredient

LANREOTIDE ACETATE

Application Number

217193

Product Number

3

Dosage Form

-

Strength

EQ 120MG BASE/0.5ML (EQ 120MG BASE/0.5ML)

Approval Date

2024-05-21

Regulatory Status

RX

2022
24 Jan
RX Application: 206868

Drug Name

LANTHANUM CARBONATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2022-01-24

206868 / 1

Active Ingredient

LANTHANUM CARBONATE

Application Number

206868

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2022-01-24

Regulatory Status

RX

2022
24 Jan
RX Application: 206868

Drug Name

LANTHANUM CARBONATE

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2022-01-24

206868 / 2

Active Ingredient

LANTHANUM CARBONATE

Application Number

206868

Product Number

2

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2022-01-24

Regulatory Status

RX

2022
24 Jan
RX Application: 206868

Drug Name

LANTHANUM CARBONATE

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2022-01-24

206868 / 3

Active Ingredient

LANTHANUM CARBONATE

Application Number

206868

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE

Approval Date

2022-01-24

Regulatory Status

RX

2018
28 Aug
RX Application: 205054

Drug Name

LEUPROLIDE ACETATE FOR DEPOT SUSPENSION

Product Number

1

Dosage Form

-

Strength

22.5MG/VIAL

Approval Date

2018-08-28

205054 / 1

Active Ingredient

LEUPROLIDE ACETATE

Application Number

205054

Product Number

1

Dosage Form

-

Strength

22.5MG/VIAL

Approval Date

2018-08-28

Regulatory Status

RX

2009
15 Jan
Discontinued Application: 78234

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2009-01-15

78234 / 1

Active Ingredient

LEVETIRACETAM

Application Number

78234

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2009-01-15

Regulatory Status

Discontinued

2009
15 Jan
Discontinued Application: 78234

Drug Name

LEVETIRACETAM

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2009-01-15

78234 / 2

Active Ingredient

LEVETIRACETAM

Application Number

78234

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2009-01-15

Regulatory Status

Discontinued

2009
15 Jan
Discontinued Application: 78234

Drug Name

LEVETIRACETAM

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2009-01-15

78234 / 3

Active Ingredient

LEVETIRACETAM

Application Number

78234

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2009-01-15

Regulatory Status

Discontinued

2024
03 Sep
RX Application: 208423

Drug Name

LINAGLIPTIN

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-09-03

208423 / 1

Active Ingredient

LINAGLIPTIN

Application Number

208423

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2024-09-03

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-10-29

203508 / 1

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-10-29

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-10-29

203508 / 2

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-10-29

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2013-10-29

203508 / 3

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2013-10-29

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2013-10-29

203508 / 4

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2013-10-29

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2013-10-29

203508 / 5

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2013-10-29

Regulatory Status

RX

2013
29 Oct
RX Application: 203508

Drug Name

LISINOPRIL

Product Number

6

Dosage Form

-

Strength

40MG

Approval Date

2013-10-29

203508 / 6

Active Ingredient

LISINOPRIL

Application Number

203508

Product Number

6

Dosage Form

-

Strength

40MG

Approval Date

2013-10-29

Regulatory Status

RX

2017
23 May
RX Application: 204058

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;10MG

Approval Date

2017-05-23

204058 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

204058

Product Number

1

Dosage Form

-

Strength

12.5MG;10MG

Approval Date

2017-05-23

Regulatory Status

RX

2017
23 May
RX Application: 204058

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;20MG

Approval Date

2017-05-23

204058 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

204058

Product Number

2

Dosage Form

-

Strength

12.5MG;20MG

Approval Date

2017-05-23

Regulatory Status

RX

2017
23 May
RX Application: 204058

Drug Name

LISINOPRIL AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;20MG

Approval Date

2017-05-23

204058 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; LISINOPRIL

Application Number

204058

Product Number

3

Dosage Form

-

Strength

25MG;20MG

Approval Date

2017-05-23

Regulatory Status

RX

2019
03 Jan
RX Application: 208028

Drug Name

LURASIDONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-01-03

208028 / 1

Active Ingredient

LURASIDONE HYDROCHLORIDE

Application Number

208028

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2019-01-03

Regulatory Status

RX

2019
03 Jan
RX Application: 208028

Drug Name

LURASIDONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2019-01-03

208028 / 2

Active Ingredient

LURASIDONE HYDROCHLORIDE

Application Number

208028

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2019-01-03

Regulatory Status

RX

2019
03 Jan
RX Application: 208028

Drug Name

LURASIDONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

60MG

Approval Date

2019-01-03

208028 / 3

Active Ingredient

LURASIDONE HYDROCHLORIDE

Application Number

208028

Product Number

3

Dosage Form

-

Strength

60MG

Approval Date

2019-01-03

Regulatory Status

RX

2019
03 Jan
RX Application: 208028

Drug Name

LURASIDONE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

80MG

Approval Date

2019-01-03

208028 / 4

Active Ingredient

LURASIDONE HYDROCHLORIDE

Application Number

208028

Product Number

4

Dosage Form

-

Strength

80MG

Approval Date

2019-01-03

Regulatory Status

RX

2019
03 Jan
RX Application: 208028

Drug Name

LURASIDONE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

120MG

Approval Date

2019-01-03

208028 / 5

Active Ingredient

LURASIDONE HYDROCHLORIDE

Application Number

208028

Product Number

5

Dosage Form

-

Strength

120MG

Approval Date

2019-01-03

Regulatory Status

RX

2022
17 Feb
Discontinued Application: 200432

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2022-02-17

200432 / 1

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

200432

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2022-02-17

Regulatory Status

Discontinued

2022
17 Feb
Discontinued Application: 200432

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2022-02-17

200432 / 2

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

200432

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

2022-02-17

Regulatory Status

Discontinued

2022
17 Feb
Discontinued Application: 200432

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2022-02-17

200432 / 3

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

200432

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2022-02-17

Regulatory Status

Discontinued

2022
17 Feb
Discontinued Application: 200791

Drug Name

MECLIZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2022-02-17

200791 / 1

Active Ingredient

MECLIZINE HYDROCHLORIDE

Application Number

200791

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2022-02-17

Regulatory Status

Discontinued

2008
27 Feb
RX Application: 40797

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2008-02-27

40797 / 1

Active Ingredient

MEPROBAMATE

Application Number

40797

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2008-02-27

Regulatory Status

RX

2008
27 Feb
RX Application: 40797

Drug Name

MEPROBAMATE

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2008-02-27

40797 / 2

Active Ingredient

MEPROBAMATE

Application Number

40797

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2008-02-27

Regulatory Status

RX

2008
07 Mar
RX Application: 78671

Drug Name

NABUMETONE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2008-03-07

78671 / 1

Active Ingredient

NABUMETONE

Application Number

78671

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2008-03-07

Regulatory Status

RX

2008
07 Mar
RX Application: 78671

Drug Name

NABUMETONE

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2008-03-07

78671 / 2

Active Ingredient

NABUMETONE

Application Number

78671

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2008-03-07

Regulatory Status

RX

2015
18 Dec
RX Application: 203455

Drug Name

NADOLOL

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2015-12-18

203455 / 1

Active Ingredient

NADOLOL

Application Number

203455

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2015-12-18

Regulatory Status

RX

2015
18 Dec
RX Application: 203455

Drug Name

NADOLOL

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2015-12-18

203455 / 2

Active Ingredient

NADOLOL

Application Number

203455

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2015-12-18

Regulatory Status

RX

2015
18 Dec
RX Application: 203455

Drug Name

NADOLOL

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

2015-12-18

203455 / 3

Active Ingredient

NADOLOL

Application Number

203455

Product Number

3

Dosage Form

-

Strength

80MG

Approval Date

2015-12-18

Regulatory Status

RX

2011
24 Aug
Discontinued Application: 91305

Drug Name

NAPROXEN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2011-08-24

91305 / 1

Active Ingredient

NAPROXEN

Application Number

91305

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2011-08-24

Regulatory Status

Discontinued

2011
24 Aug
Discontinued Application: 91305

Drug Name

NAPROXEN

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

2011-08-24

91305 / 2

Active Ingredient

NAPROXEN

Application Number

91305

Product Number

2

Dosage Form

-

Strength

375MG

Approval Date

2011-08-24

Regulatory Status

Discontinued

2011
24 Aug
Discontinued Application: 91305

Drug Name

NAPROXEN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2011-08-24

91305 / 3

Active Ingredient

NAPROXEN

Application Number

91305

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

2011-08-24

Regulatory Status

Discontinued

2021
30 Aug
RX Application: 212858

Drug Name

OSELTAMIVIR PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2021-08-30

212858 / 1

Active Ingredient

OSELTAMIVIR PHOSPHATE

Application Number

212858

Product Number

1

Dosage Form

-

Strength

EQ 6MG BASE/ML

Approval Date

2021-08-30

Regulatory Status

RX

2023
03 Oct
RX Application: 217467

Drug Name

OSELTAMIVIR PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2023-10-03

217467 / 1

Active Ingredient

OSELTAMIVIR PHOSPHATE

Application Number

217467

Product Number

1

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2023-10-03

Regulatory Status

RX

2023
03 Oct
RX Application: 217467

Drug Name

OSELTAMIVIR PHOSPHATE

Product Number

2

Dosage Form

-

Strength

EQ 45MG BASE

Approval Date

2023-10-03

217467 / 2

Active Ingredient

OSELTAMIVIR PHOSPHATE

Application Number

217467

Product Number

2

Dosage Form

-

Strength

EQ 45MG BASE

Approval Date

2023-10-03

Regulatory Status

RX

2023
03 Oct
RX Application: 217467

Drug Name

OSELTAMIVIR PHOSPHATE

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2023-10-03

217467 / 3

Active Ingredient

OSELTAMIVIR PHOSPHATE

Application Number

217467

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2023-10-03

Regulatory Status

RX

2021
19 Aug
RX Application: 213293

Drug Name

PENICILLAMINE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2021-08-19

213293 / 1

Active Ingredient

PENICILLAMINE

Application Number

213293

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2021-08-19

Regulatory Status

RX

2014
05 Feb
Discontinued Application: 202846

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2014-02-05

202846 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

202846

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2014-02-05

Regulatory Status

Discontinued

2014
14 Feb
Discontinued Application: 202858

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2014-02-14

202858 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

202858

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2014-02-14

Regulatory Status

Discontinued

2014
14 Feb
Discontinued Application: 202858

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2014-02-14

202858 / 2

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

202858

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2014-02-14

Regulatory Status

Discontinued

2014
05 Feb
Discontinued Application: 202942

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2014-02-05

202942 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

202942

Product Number

1

Dosage Form

-

Strength

37.5MG

Approval Date

2014-02-05

Regulatory Status

Discontinued

2014
05 May
Discontinued Application: 204414

Drug Name

PHENTERMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2014-05-05

204414 / 1

Active Ingredient

PHENTERMINE HYDROCHLORIDE

Application Number

204414

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2014-05-05

Regulatory Status

Discontinued

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2019-07-19

211384 / 1

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2019-07-19

211384 / 2

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2019-07-19

211384 / 3

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2019-07-19

211384 / 4

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

4

Dosage Form

-

Strength

100MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

5

Dosage Form

-

Strength

150MG

Approval Date

2019-07-19

211384 / 5

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

5

Dosage Form

-

Strength

150MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

6

Dosage Form

-

Strength

200MG

Approval Date

2019-07-19

211384 / 6

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

6

Dosage Form

-

Strength

200MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

7

Dosage Form

-

Strength

225MG

Approval Date

2019-07-19

211384 / 7

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

7

Dosage Form

-

Strength

225MG

Approval Date

2019-07-19

Regulatory Status

RX

2019
19 Jul
RX Application: 211384

Drug Name

PREGABALIN

Product Number

8

Dosage Form

-

Strength

300MG

Approval Date

2019-07-19

211384 / 8

Active Ingredient

PREGABALIN

Application Number

211384

Product Number

8

Dosage Form

-

Strength

300MG

Approval Date

2019-07-19

Regulatory Status

RX

2007
24 Aug
Discontinued Application: 78457

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-08-24

78457 / 1

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

78457

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-08-24

Regulatory Status

Discontinued

2007
24 Aug
Discontinued Application: 78457

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-08-24

78457 / 2

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

78457

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-08-24

Regulatory Status

Discontinued

2007
24 Aug
Discontinued Application: 78457

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2007-08-24

78457 / 3

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

78457

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2007-08-24

Regulatory Status

Discontinued

2007
24 Aug
Discontinued Application: 78457

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-08-24

78457 / 4

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

78457

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-08-24

Regulatory Status

Discontinued

2011
20 Apr
Discontinued Application: 201356

Drug Name

QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;EQ 10MG BASE

Approval Date

2011-04-20

201356 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Application Number

201356

Product Number

1

Dosage Form

-

Strength

12.5MG;EQ 10MG BASE

Approval Date

2011-04-20

Regulatory Status

Discontinued

2011
20 Apr
Discontinued Application: 201356

Drug Name

QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;EQ 20MG BASE

Approval Date

2011-04-20

201356 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Application Number

201356

Product Number

2

Dosage Form

-

Strength

12.5MG;EQ 20MG BASE

Approval Date

2011-04-20

Regulatory Status

Discontinued

2011
20 Apr
Discontinued Application: 201356

Drug Name

QUINAPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

25MG;EQ 20MG BASE

Approval Date

2011-04-20

201356 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

Application Number

201356

Product Number

3

Dosage Form

-

Strength

25MG;EQ 20MG BASE

Approval Date

2011-04-20

Regulatory Status

Discontinued

2014
24 Sep
RX Application: 90842

Drug Name

RALOXIFENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2014-09-24

90842 / 1

Active Ingredient

RALOXIFENE HYDROCHLORIDE

Application Number

90842

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2014-09-24

Regulatory Status

RX

2025
14 May
Discontinued Application: 208543

Drug Name

RIVAROXABAN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2025-05-14

208543 / 1

Active Ingredient

RIVAROXABAN

Application Number

208543

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2025-05-14

Regulatory Status

Discontinued

2025
14 May
Discontinued Application: 208543

Drug Name

RIVAROXABAN

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2025-05-14

208543 / 2

Active Ingredient

RIVAROXABAN

Application Number

208543

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2025-05-14

Regulatory Status

Discontinued

2025
14 May
Discontinued Application: 208543

Drug Name

RIVAROXABAN

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2025-05-14

208543 / 3

Active Ingredient

RIVAROXABAN

Application Number

208543

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2025-05-14

Regulatory Status

Discontinued

2026
20 Feb
RX Application: 218768

Drug Name

RIVAROXABAN

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2026-02-20

218768 / 1

Active Ingredient

RIVAROXABAN

Application Number

218768

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2026-02-20

Regulatory Status

RX

2013
01 Jul
Discontinued Application: 204339

Drug Name

RIZATRIPTAN BENZOATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2013-07-01

204339 / 1

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

204339

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2013-07-01

Regulatory Status

Discontinued

2013
01 Jul
Discontinued Application: 204339

Drug Name

RIZATRIPTAN BENZOATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2013-07-01

204339 / 2

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

204339

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2013-07-01

Regulatory Status

Discontinued

2007
06 Feb
RX Application: 77397

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2007-02-06

77397 / 1

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

77397

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2007-02-06

Regulatory Status

RX

2007
06 Feb
RX Application: 77397

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2007-02-06

77397 / 2

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

77397

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2007-02-06

Regulatory Status

RX

2007
06 Feb
RX Application: 77397

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2007-02-06

77397 / 3

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

77397

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2007-02-06

Regulatory Status

RX

2017
26 Oct
RX Application: 203860

Drug Name

SEVELAMER CARBONATE

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

2017-10-26

203860 / 1

Active Ingredient

SEVELAMER CARBONATE

Application Number

203860

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

2017-10-26

Regulatory Status

RX

2024
12 Jul
Discontinued Application: 206234

Drug Name

SEVELAMER CARBONATE

Product Number

1

Dosage Form

-

Strength

800MG/PACKET

Approval Date

2024-07-12

206234 / 1

Active Ingredient

SEVELAMER CARBONATE

Application Number

206234

Product Number

1

Dosage Form

-

Strength

800MG/PACKET

Approval Date

2024-07-12

Regulatory Status

Discontinued

2024
12 Jul
Discontinued Application: 206234

Drug Name

SEVELAMER CARBONATE

Product Number

2

Dosage Form

-

Strength

2.4GM/PACKET

Approval Date

2024-07-12

206234 / 2

Active Ingredient

SEVELAMER CARBONATE

Application Number

206234

Product Number

2

Dosage Form

-

Strength

2.4GM/PACKET

Approval Date

2024-07-12

Regulatory Status

Discontinued

2020
06 Aug
RX Application: 213041

Drug Name

SILDENAFIL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2020-08-06

213041 / 1

Active Ingredient

SILDENAFIL CITRATE

Application Number

213041

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2020-08-06

Regulatory Status

RX

2017
13 Nov
RX Application: 206557

Drug Name

SIMVASTATIN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2017-11-13

206557 / 1

Active Ingredient

SIMVASTATIN

Application Number

206557

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2017-11-13

Regulatory Status

RX

2017
13 Nov
RX Application: 206557

Drug Name

SIMVASTATIN

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2017-11-13

206557 / 2

Active Ingredient

SIMVASTATIN

Application Number

206557

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2017-11-13

Regulatory Status

RX

2017
13 Nov
RX Application: 206557

Drug Name

SIMVASTATIN

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2017-11-13

206557 / 3

Active Ingredient

SIMVASTATIN

Application Number

206557

Product Number

3

Dosage Form

-

Strength

40MG

Approval Date

2017-11-13

Regulatory Status

RX

2017
13 Nov
RX Application: 206557

Drug Name

SIMVASTATIN

Product Number

4

Dosage Form

-

Strength

80MG

Approval Date

2017-11-13

206557 / 4

Active Ingredient

SIMVASTATIN

Application Number

206557

Product Number

4

Dosage Form

-

Strength

80MG

Approval Date

2017-11-13

Regulatory Status

RX

2025
27 Oct
RX Application: 206557

Drug Name

SIMVASTATIN

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

2025-10-27

206557 / 5

Active Ingredient

SIMVASTATIN

Application Number

206557

Product Number

5

Dosage Form

-

Strength

5MG

Approval Date

2025-10-27

Regulatory Status

RX

2007
02 Jul
Discontinued Application: 77533

Drug Name

TERBINAFINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2007-07-02

77533 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

77533

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2007-07-02

Regulatory Status

Discontinued

2025
05 May
RX Application: 208537

Drug Name

TICAGRELOR

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

2025-05-05

208537 / 1

Active Ingredient

TICAGRELOR

Application Number

208537

Product Number

1

Dosage Form

-

Strength

90MG

Approval Date

2025-05-05

Regulatory Status

RX

2025
28 Oct
RX Application: 208537

Drug Name

TICAGRELOR

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2025-10-28

208537 / 2

Active Ingredient

TICAGRELOR

Application Number

208537

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2025-10-28

Regulatory Status

RX

2009
27 Mar
RX Application: 79162

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

79162 / 1

Active Ingredient

TOPIRAMATE

Application Number

79162

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2009-03-27

Regulatory Status

RX

2009
27 Mar
RX Application: 79162

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2009-03-27

79162 / 2

Active Ingredient

TOPIRAMATE

Application Number

79162

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2009-03-27

Regulatory Status

RX

2009
27 Mar
RX Application: 79162

Drug Name

TOPIRAMATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

79162 / 3

Active Ingredient

TOPIRAMATE

Application Number

79162

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2009-03-27

Regulatory Status

RX

2009
27 Mar
RX Application: 79162

Drug Name

TOPIRAMATE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

79162 / 4

Active Ingredient

TOPIRAMATE

Application Number

79162

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2009-03-27

Regulatory Status

RX

2007
12 Jun
Discontinued Application: 78320

Drug Name

TRANDOLAPRIL

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2007-06-12

78320 / 1

Active Ingredient

TRANDOLAPRIL

Application Number

78320

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2007-06-12

Regulatory Status

Discontinued

2007
12 Jun
Discontinued Application: 78320

Drug Name

TRANDOLAPRIL

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2007-06-12

78320 / 2

Active Ingredient

TRANDOLAPRIL

Application Number

78320

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2007-06-12

Regulatory Status

Discontinued

2007
12 Jun
Discontinued Application: 78320

Drug Name

TRANDOLAPRIL

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2007-06-12

78320 / 3

Active Ingredient

TRANDOLAPRIL

Application Number

78320

Product Number

3

Dosage Form

-

Strength

4MG

Approval Date

2007-06-12

Regulatory Status

Discontinued

2016
23 Aug
RX Application: 91688

Drug Name

TROSPIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2016-08-23

91688 / 1

Active Ingredient

TROSPIUM CHLORIDE

Application Number

91688

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2016-08-23

Regulatory Status

RX

2019
03 Dec
RX Application: 211592

Drug Name

VIGABATRIN

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2019-12-03

211592 / 1

Active Ingredient

VIGABATRIN

Application Number

211592

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2019-12-03

Regulatory Status

RX

2021
07 Apr
RX Application: 208200

Drug Name

VILAZODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-04-07

208200 / 1

Active Ingredient

VILAZODONE HYDROCHLORIDE

Application Number

208200

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-04-07

Regulatory Status

RX

2021
07 Apr
RX Application: 208200

Drug Name

VILAZODONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2021-04-07

208200 / 2

Active Ingredient

VILAZODONE HYDROCHLORIDE

Application Number

208200

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2021-04-07

Regulatory Status

RX

2022
06 Dec
RX Application: 208200

Drug Name

VILAZODONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2022-12-06

208200 / 3

Active Ingredient

VILAZODONE HYDROCHLORIDE

Application Number

208200

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

2022-12-06

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2011-05-25

90935 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2011-05-25

90935 / 2

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

2011-05-25

90935 / 3

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

3

Dosage Form

-

Strength

2.5MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2011-05-25

90935 / 4

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

4

Dosage Form

-

Strength

3MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

5

Dosage Form

-

Strength

4MG

Approval Date

2011-05-25

90935 / 5

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

5

Dosage Form

-

Strength

4MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

6

Dosage Form

-

Strength

5MG

Approval Date

2011-05-25

90935 / 6

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

6

Dosage Form

-

Strength

5MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

7

Dosage Form

-

Strength

6MG

Approval Date

2011-05-25

90935 / 7

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

7

Dosage Form

-

Strength

6MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

8

Dosage Form

-

Strength

7.5MG

Approval Date

2011-05-25

90935 / 8

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

8

Dosage Form

-

Strength

7.5MG

Approval Date

2011-05-25

Regulatory Status

RX

2011
25 May
RX Application: 90935

Drug Name

WARFARIN SODIUM

Product Number

9

Dosage Form

-

Strength

10MG

Approval Date

2011-05-25

90935 / 9

Active Ingredient

WARFARIN SODIUM

Application Number

90935

Product Number

9

Dosage Form

-

Strength

10MG

Approval Date

2011-05-25

Regulatory Status

RX

2014
09 Apr
Discontinued Application: 204284

Drug Name

ZOLMITRIPTAN

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2014-04-09

204284 / 1

Active Ingredient

ZOLMITRIPTAN

Application Number

204284

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2014-04-09

Regulatory Status

Discontinued

2014
09 Apr
Discontinued Application: 204284

Drug Name

ZOLMITRIPTAN

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2014-04-09

204284 / 2

Active Ingredient

ZOLMITRIPTAN

Application Number

204284

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2014-04-09

Regulatory Status

Discontinued

2007
07 Sep
Discontinued Application: 78184

Drug Name

ZOLPIDEM TARTRATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-09-07

78184 / 1

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

78184

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-09-07

Regulatory Status

Discontinued

2007
07 Sep
Discontinued Application: 78184

Drug Name

ZOLPIDEM TARTRATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-09-07

78184 / 2

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

78184

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-09-07

Regulatory Status

Discontinued

2006
31 May
RX Application: 77869

Drug Name

ZONISAMIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2006-05-31

77869 / 1

Active Ingredient

ZONISAMIDE

Application Number

77869

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2006-05-31

Regulatory Status

RX

2006
31 May
RX Application: 77869

Drug Name

ZONISAMIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2006-05-31

77869 / 2

Active Ingredient

ZONISAMIDE

Application Number

77869

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2006-05-31

Regulatory Status

RX

2006
31 May
RX Application: 77869

Drug Name

ZONISAMIDE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2006-05-31

77869 / 3

Active Ingredient

ZONISAMIDE

Application Number

77869

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2006-05-31

Regulatory Status

RX

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    170 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
170 total
  • RX
  • Discontinued
  • Unclassified
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ALFUZOSIN HYDROCHLORIDE

Application Number

90284

Product Number

1

Active Ingredient

ALFUZOSIN HYDROCHLORIDE

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit