Apotex Inc Discontinued
FDA Approved Drugs

Apotex Inc Discontinued

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.

Discontinued
  • Total Records 114
  • Latest Approval Date Dec 23, 2015
  • Data Source FDA
  • First Approval Date Apr 29, 1998
All
194
View
Unclassified
38
View
Discontinued
114
View
OTC
2
View
RX
40
View
Company Overview

Company

Apotex Inc Discontinued

Country

Canada

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Company Snapshot

Apotex Inc Discontinued

150 Signet Drive, Toronto, Ontario, M9L 1T9

Canada

www.apotex.com/global/error-pages?initialRequestUrl=https%3a%2f%2fwww.apotex.com%2fglobal%2fdefault.asp View on Map
FDA Approved Drug Records ( 114 records )
2012
17 Dec
Discontinued Application: 201570

Drug Name

ABACAVIR SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2012-12-17

201570 / 1

Active Ingredient

ABACAVIR SULFATE

Application Number

201570

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE

Approval Date

2012-12-17

Regulatory Status

Discontinued

2007
02 Feb
Discontinued Application: 75717

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2007-02-02

75717 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

75717

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2007-02-02

Regulatory Status

Discontinued

2003
01 Apr
Discontinued Application: 76391

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2003-04-01

76391 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

76391

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2003-04-01

Regulatory Status

Discontinued

2010
05 Apr
Discontinued Application: 78623

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2010-04-05

78623 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

78623

Product Number

1

Dosage Form

-

Strength

EQ 0.021% BASE

Approval Date

2010-04-05

Regulatory Status

Discontinued

2010
05 Apr
Discontinued Application: 78623

Drug Name

ALBUTEROL SULFATE

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2010-04-05

78623 / 2

Active Ingredient

ALBUTEROL SULFATE

Application Number

78623

Product Number

2

Dosage Form

-

Strength

EQ 0.042% BASE

Approval Date

2010-04-05

Regulatory Status

Discontinued

2007
31 Dec
Discontinued Application: 77117

Drug Name

ALBUTEROL SULFATE AND IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2007-12-31

77117 / 1

Active Ingredient

ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

Application Number

77117

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE;0.017%

Approval Date

2007-12-31

Regulatory Status

Discontinued

2007
19 Jan
Discontinued Application: 77741

Drug Name

ALPRAZOLAM

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2007-01-19

77741 / 1

Active Ingredient

ALPRAZOLAM

Application Number

77741

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2007-01-19

Regulatory Status

Discontinued

2007
19 Jan
Discontinued Application: 77741

Drug Name

ALPRAZOLAM

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2007-01-19

77741 / 2

Active Ingredient

ALPRAZOLAM

Application Number

77741

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2007-01-19

Regulatory Status

Discontinued

2007
19 Jan
Discontinued Application: 77741

Drug Name

ALPRAZOLAM

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2007-01-19

77741 / 3

Active Ingredient

ALPRAZOLAM

Application Number

77741

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2007-01-19

Regulatory Status

Discontinued

2007
19 Jan
Discontinued Application: 77741

Drug Name

ALPRAZOLAM

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2007-01-19

77741 / 4

Active Ingredient

ALPRAZOLAM

Application Number

77741

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2007-01-19

Regulatory Status

Discontinued

2008
12 Nov
Discontinued Application: 78449

Drug Name

ALPRAZOLAM

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2008-11-12

78449 / 1

Active Ingredient

ALPRAZOLAM

Application Number

78449

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2008-11-12

Regulatory Status

Discontinued

2008
12 Nov
Discontinued Application: 78449

Drug Name

ALPRAZOLAM

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2008-11-12

78449 / 2

Active Ingredient

ALPRAZOLAM

Application Number

78449

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2008-11-12

Regulatory Status

Discontinued

2008
12 Nov
Discontinued Application: 78449

Drug Name

ALPRAZOLAM

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

2008-11-12

78449 / 3

Active Ingredient

ALPRAZOLAM

Application Number

78449

Product Number

3

Dosage Form

-

Strength

3MG

Approval Date

2008-11-12

Regulatory Status

Discontinued

2015
23 Dec
Discontinued Application: 78449

Drug Name

ALPRAZOLAM

Product Number

4

Dosage Form

-

Strength

1MG

Approval Date

2015-12-23

78449 / 4

Active Ingredient

ALPRAZOLAM

Application Number

78449

Product Number

4

Dosage Form

-

Strength

1MG

Approval Date

2015-12-23

Regulatory Status

Discontinued

2008
20 Oct
Discontinued Application: 65317

Drug Name

AMOXICILLIN AND CLAVULANATE POTASSIUM

Product Number

3

Dosage Form

-

Strength

875MG;EQ 125MG BASE

Approval Date

2008-10-20

65317 / 3

Active Ingredient

AMOXICILLIN; CLAVULANATE POTASSIUM

Application Number

65317

Product Number

3

Dosage Form

-

Strength

875MG;EQ 125MG BASE

Approval Date

2008-10-20

Regulatory Status

Discontinued

2009
24 Feb
Discontinued Application: 65333

Drug Name

AMOXICILLIN AND CLAVULANATE POTASSIUM

Product Number

1

Dosage Form

-

Strength

250MG;EQ 125MG BASE

Approval Date

2009-02-24

65333 / 1

Active Ingredient

AMOXICILLIN; CLAVULANATE POTASSIUM

Application Number

65333

Product Number

1

Dosage Form

-

Strength

250MG;EQ 125MG BASE

Approval Date

2009-02-24

Regulatory Status

Discontinued

2009
24 Feb
Discontinued Application: 65333

Drug Name

AMOXICILLIN AND CLAVULANATE POTASSIUM

Product Number

2

Dosage Form

-

Strength

500MG;EQ 125MG BASE

Approval Date

2009-02-24

65333 / 2

Active Ingredient

AMOXICILLIN; CLAVULANATE POTASSIUM

Application Number

65333

Product Number

2

Dosage Form

-

Strength

500MG;EQ 125MG BASE

Approval Date

2009-02-24

Regulatory Status

Discontinued

2012
11 May
Discontinued Application: 200654

Drug Name

ANASTROZOLE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2012-05-11

200654 / 1

Active Ingredient

ANASTROZOLE

Application Number

200654

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2012-05-11

Regulatory Status

Discontinued

2012
31 Aug
Discontinued Application: 201846

Drug Name

AZELASTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2055MG/SPRAY

Approval Date

2012-08-31

201846 / 1

Active Ingredient

AZELASTINE HYDROCHLORIDE

Application Number

201846

Product Number

1

Dosage Form

-

Strength

0.2055MG/SPRAY

Approval Date

2012-08-31

Regulatory Status

Discontinued

2000
28 Sep
Discontinued Application: 75446

Drug Name

BETAXOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2000-09-28

75446 / 1

Active Ingredient

BETAXOLOL HYDROCHLORIDE

Application Number

75446

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2000-09-28

Regulatory Status

Discontinued

2012
04 Dec
Discontinued Application: 202884

Drug Name

CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

16MG;12.5MG

Approval Date

2012-12-04

202884 / 1

Active Ingredient

CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE

Application Number

202884

Product Number

1

Dosage Form

-

Strength

16MG;12.5MG

Approval Date

2012-12-04

Regulatory Status

Discontinued

2012
04 Dec
Discontinued Application: 202884

Drug Name

CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

32MG;12.5MG

Approval Date

2012-12-04

202884 / 2

Active Ingredient

CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE

Application Number

202884

Product Number

2

Dosage Form

-

Strength

32MG;12.5MG

Approval Date

2012-12-04

Regulatory Status

Discontinued

2013
03 Jun
Discontinued Application: 202884

Drug Name

CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

32MG;25MG

Approval Date

2013-06-03

202884 / 3

Active Ingredient

CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE

Application Number

202884

Product Number

3

Dosage Form

-

Strength

32MG;25MG

Approval Date

2013-06-03

Regulatory Status

Discontinued

2008
02 Jun
Discontinued Application: 77120

Drug Name

CARBIDOPA AND LEVODOPA

Product Number

1

Dosage Form

-

Strength

10MG;100MG

Approval Date

2008-06-02

77120 / 1

Active Ingredient

CARBIDOPA; LEVODOPA

Application Number

77120

Product Number

1

Dosage Form

-

Strength

10MG;100MG

Approval Date

2008-06-02

Regulatory Status

Discontinued

2008
02 Jun
Discontinued Application: 77120

Drug Name

CARBIDOPA AND LEVODOPA

Product Number

2

Dosage Form

-

Strength

25MG;100MG

Approval Date

2008-06-02

77120 / 2

Active Ingredient

CARBIDOPA; LEVODOPA

Application Number

77120

Product Number

2

Dosage Form

-

Strength

25MG;100MG

Approval Date

2008-06-02

Regulatory Status

Discontinued

2008
02 Jun
Discontinued Application: 77120

Drug Name

CARBIDOPA AND LEVODOPA

Product Number

3

Dosage Form

-

Strength

25MG;250MG

Approval Date

2008-06-02

77120 / 3

Active Ingredient

CARBIDOPA; LEVODOPA

Application Number

77120

Product Number

3

Dosage Form

-

Strength

25MG;250MG

Approval Date

2008-06-02

Regulatory Status

Discontinued

2002
06 Feb
Discontinued Application: 76097

Drug Name

CARTEOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2002-02-06

76097 / 1

Active Ingredient

CARTEOLOL HYDROCHLORIDE

Application Number

76097

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2002-02-06

Regulatory Status

Discontinued

2008
26 Mar
Discontinued Application: 65327

Drug Name

CEFPROZIL

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2008-03-26

65327 / 1

Active Ingredient

CEFPROZIL

Application Number

65327

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2008-03-26

Regulatory Status

Discontinued

2008
26 Mar
Discontinued Application: 65327

Drug Name

CEFPROZIL

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2008-03-26

65327 / 2

Active Ingredient

CEFPROZIL

Application Number

65327

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2008-03-26

Regulatory Status

Discontinued

2012
29 Feb
Discontinued Application: 65351

Drug Name

CEFPROZIL

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

2012-02-29

65351 / 1

Active Ingredient

CEFPROZIL

Application Number

65351

Product Number

1

Dosage Form

-

Strength

125MG/5ML

Approval Date

2012-02-29

Regulatory Status

Discontinued

2012
29 Feb
Discontinued Application: 65351

Drug Name

CEFPROZIL

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

2012-02-29

65351 / 2

Active Ingredient

CEFPROZIL

Application Number

65351

Product Number

2

Dosage Form

-

Strength

250MG/5ML

Approval Date

2012-02-29

Regulatory Status

Discontinued

2011
25 Aug
Discontinued Application: 91260

Drug Name

CEVIMELINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2011-08-25

91260 / 1

Active Ingredient

CEVIMELINE HYDROCHLORIDE

Application Number

91260

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2011-08-25

Regulatory Status

Discontinued

2000
27 Nov
Discontinued Application: 75703

Drug Name

CLEMASTINE FUMARATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5MG BASE/5ML

Approval Date

2000-11-27

75703 / 1

Active Ingredient

CLEMASTINE FUMARATE

Application Number

75703

Product Number

1

Dosage Form

-

Strength

EQ 0.5MG BASE/5ML

Approval Date

2000-11-27

Regulatory Status

Discontinued

2001
26 Jan
Discontinued Application: 75615

Drug Name

CROMOLYN SODIUM

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

2001-01-26

75615 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

75615

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

2001-01-26

Regulatory Status

Discontinued

2012
11 Jan
Discontinued Application: 22312

Drug Name

DOCETAXEL

Product Number

1

Dosage Form

-

Strength

20MG/0.5ML (40MG/ML)

Approval Date

2012-01-11

22312 / 1

Active Ingredient

DOCETAXEL

Application Number

22312

Product Number

1

Dosage Form

-

Strength

20MG/0.5ML (40MG/ML)

Approval Date

2012-01-11

Regulatory Status

Discontinued

2012
11 Jan
Discontinued Application: 22312

Drug Name

DOCETAXEL

Product Number

2

Dosage Form

-

Strength

80MG/2ML (40MG/ML)

Approval Date

2012-01-11

22312 / 2

Active Ingredient

DOCETAXEL

Application Number

22312

Product Number

2

Dosage Form

-

Strength

80MG/2ML (40MG/ML)

Approval Date

2012-01-11

Regulatory Status

Discontinued

2002
02 Aug
Discontinued Application: 75942

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2002-08-02

75942 / 1

Active Ingredient

FAMOTIDINE

Application Number

75942

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

2002-08-02

Regulatory Status

Discontinued

2007
06 Aug
Discontinued Application: 78126

Drug Name

FOSPHENYTOIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG PHENYTOIN NA/ML

Approval Date

2007-08-06

78126 / 1

Active Ingredient

FOSPHENYTOIN SODIUM

Application Number

78126

Product Number

1

Dosage Form

-

Strength

EQ 50MG PHENYTOIN NA/ML

Approval Date

2007-08-06

Regulatory Status

Discontinued

2011
27 Sep
Discontinued Application: 77781

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2011-09-27

77781 / 1

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77781

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2011-09-27

Regulatory Status

Discontinued

2011
27 Sep
Discontinued Application: 77781

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2011-09-27

77781 / 2

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77781

Product Number

2

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2011-09-27

Regulatory Status

Discontinued

2011
27 Sep
Discontinued Application: 77781

Drug Name

GALANTAMINE HYDROBROMIDE

Product Number

3

Dosage Form

-

Strength

EQ 12MG BASE

Approval Date

2011-09-27

77781 / 3

Active Ingredient

GALANTAMINE HYDROBROMIDE

Application Number

77781

Product Number

3

Dosage Form

-

Strength

EQ 12MG BASE

Approval Date

2011-09-27

Regulatory Status

Discontinued

2011
19 Aug
Discontinued Application: 79084

Drug Name

GATIFLOXACIN

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2011-08-19

79084 / 1

Active Ingredient

GATIFLOXACIN

Application Number

79084

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2011-08-19

Regulatory Status

Discontinued

2008
27 Feb
Discontinued Application: 78843

Drug Name

GRANISETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2008-02-27

78843 / 1

Active Ingredient

GRANISETRON HYDROCHLORIDE

Application Number

78843

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2008-02-27

Regulatory Status

Discontinued

2012
06 Apr
Discontinued Application: 91308

Drug Name

IMIQUIMOD

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2012-04-06

91308 / 1

Active Ingredient

IMIQUIMOD

Application Number

91308

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2012-04-06

Regulatory Status

Discontinued

2001
28 Mar
Discontinued Application: 75441

Drug Name

IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-03-28

75441 / 1

Active Ingredient

IPRATROPIUM BROMIDE

Application Number

75441

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2001-03-28

Regulatory Status

Discontinued

2012
15 Oct
Discontinued Application: 200832

Drug Name

IRBESARTAN

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2012-10-15

200832 / 1

Active Ingredient

IRBESARTAN

Application Number

200832

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2012-10-15

Regulatory Status

Discontinued

2012
15 Oct
Discontinued Application: 200832

Drug Name

IRBESARTAN

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2012-10-15

200832 / 2

Active Ingredient

IRBESARTAN

Application Number

200832

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

2012-10-15

Regulatory Status

Discontinued

2012
15 Oct
Discontinued Application: 200832

Drug Name

IRBESARTAN

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2012-10-15

200832 / 3

Active Ingredient

IRBESARTAN

Application Number

200832

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2012-10-15

Regulatory Status

Discontinued

2012
15 Oct
Discontinued Application: 201505

Drug Name

IRBESARTAN AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;150MG

Approval Date

2012-10-15

201505 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; IRBESARTAN

Application Number

201505

Product Number

1

Dosage Form

-

Strength

12.5MG;150MG

Approval Date

2012-10-15

Regulatory Status

Discontinued

2012
15 Oct
Discontinued Application: 201505

Drug Name

IRBESARTAN AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;300MG

Approval Date

2012-10-15

201505 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; IRBESARTAN

Application Number

201505

Product Number

2

Dosage Form

-

Strength

12.5MG;300MG

Approval Date

2012-10-15

Regulatory Status

Discontinued

2001
24 Jul
Discontinued Application: 75626

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2001-07-24

75626 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

75626

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2001-07-24

Regulatory Status

Discontinued

2005
14 Oct
Discontinued Application: 77201

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2005-10-14

77201 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

77201

Product Number

1

Dosage Form

-

Strength

30MG/ML

Approval Date

2005-10-14

Regulatory Status

Discontinued

2006
09 May
Discontinued Application: 77354

Drug Name

KETOTIFEN FUMARATE

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2006-05-09

77354 / 1

Active Ingredient

KETOTIFEN FUMARATE

Application Number

77354

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2006-05-09

Regulatory Status

Discontinued

2011
22 Mar
Discontinued Application: 77697

Drug Name

LATANOPROST

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2011-03-22

77697 / 1

Active Ingredient

LATANOPROST

Application Number

77697

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2011-03-22

Regulatory Status

Discontinued

2012
19 Apr
Discontinued Application: 91303

Drug Name

LETROZOLE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2012-04-19

91303 / 1

Active Ingredient

LETROZOLE

Application Number

91303

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2012-04-19

Regulatory Status

Discontinued

2011
05 Aug
Discontinued Application: 90187

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2011-08-05

90187 / 1

Active Ingredient

LEVETIRACETAM

Application Number

90187

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2011-08-05

Regulatory Status

Discontinued

2000
03 Aug
Discontinued Application: 75473

Drug Name

LEVOBUNOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2000-08-03

75473 / 1

Active Ingredient

LEVOBUNOLOL HYDROCHLORIDE

Application Number

75473

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2000-08-03

Regulatory Status

Discontinued

2000
03 Aug
Discontinued Application: 75475

Drug Name

LEVOBUNOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2000-08-03

75475 / 1

Active Ingredient

LEVOBUNOLOL HYDROCHLORIDE

Application Number

75475

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2000-08-03

Regulatory Status

Discontinued

2011
29 Sep
Discontinued Application: 90787

Drug Name

LEVOFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2011-09-29

90787 / 1

Active Ingredient

LEVOFLOXACIN

Application Number

90787

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2011-09-29

Regulatory Status

Discontinued

2011
29 Sep
Discontinued Application: 90787

Drug Name

LEVOFLOXACIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2011-09-29

90787 / 2

Active Ingredient

LEVOFLOXACIN

Application Number

90787

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2011-09-29

Regulatory Status

Discontinued

2011
29 Sep
Discontinued Application: 90787

Drug Name

LEVOFLOXACIN

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2011-09-29

90787 / 3

Active Ingredient

LEVOFLOXACIN

Application Number

90787

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2011-09-29

Regulatory Status

Discontinued

2004
22 Nov
Discontinued Application: 76795

Drug Name

LITHIUM CARBONATE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2004-11-22

76795 / 1

Active Ingredient

LITHIUM CARBONATE

Application Number

76795

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2004-11-22

Regulatory Status

Discontinued

2000
27 Jan
Discontinued Application: 75235

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

10MG/5ML

Approval Date

2000-01-27

75235 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

75235

Product Number

1

Dosage Form

-

Strength

10MG/5ML

Approval Date

2000-01-27

Regulatory Status

Discontinued

2001
28 Feb
Discontinued Application: 75402

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

0.4%

Approval Date

2001-02-28

75402 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

75402

Product Number

1

Dosage Form

-

Strength

0.4%

Approval Date

2001-02-28

Regulatory Status

Discontinued

2001
28 Feb
Discontinued Application: 75403

Drug Name

METAPROTERENOL SULFATE

Product Number

1

Dosage Form

-

Strength

0.6%

Approval Date

2001-02-28

75403 / 1

Active Ingredient

METAPROTERENOL SULFATE

Application Number

75403

Product Number

1

Dosage Form

-

Strength

0.6%

Approval Date

2001-02-28

Regulatory Status

Discontinued

1998
29 Apr
Discontinued Application: 74924

Drug Name

MINOXIDIL (FOR MEN)

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1998-04-29

74924 / 1

Active Ingredient

MINOXIDIL

Application Number

74924

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1998-04-29

Regulatory Status

Discontinued

1998
29 Apr
Discontinued Application: 74924

Drug Name

MINOXIDIL (FOR WOMEN)

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1998-04-29

74924 / 2

Active Ingredient

MINOXIDIL

Application Number

74924

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

1998-04-29

Regulatory Status

Discontinued

2001
01 Oct
Discontinued Application: 75839

Drug Name

MINOXIDIL EXTRA STRENGTH (FOR MEN)

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2001-10-01

75839 / 1

Active Ingredient

MINOXIDIL

Application Number

75839

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2001-10-01

Regulatory Status

Discontinued

2008
02 Jun
Discontinued Application: 78454

Drug Name

MOEXIPRIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2008-06-02

78454 / 1

Active Ingredient

MOEXIPRIL HYDROCHLORIDE

Application Number

78454

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2008-06-02

Regulatory Status

Discontinued

2008
02 Jun
Discontinued Application: 78454

Drug Name

MOEXIPRIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2008-06-02

78454 / 2

Active Ingredient

MOEXIPRIL HYDROCHLORIDE

Application Number

78454

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2008-06-02

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 201508

Drug Name

MONTELUKAST SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

201508 / 1

Active Ingredient

MONTELUKAST SODIUM

Application Number

201508

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 201508

Drug Name

MONTELUKAST SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

201508 / 2

Active Ingredient

MONTELUKAST SODIUM

Application Number

201508

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

2012
22 May
Discontinued Application: 203021

Drug Name

NEVIRAPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2012-05-22

203021 / 1

Active Ingredient

NEVIRAPINE

Application Number

203021

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2012-05-22

Regulatory Status

Discontinued

2003
23 Jan
Discontinued Application: 76383

Drug Name

NIZATIDINE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2003-01-23

76383 / 1

Active Ingredient

NIZATIDINE

Application Number

76383

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2003-01-23

Regulatory Status

Discontinued

2003
23 Jan
Discontinued Application: 76383

Drug Name

NIZATIDINE

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2003-01-23

76383 / 2

Active Ingredient

NIZATIDINE

Application Number

76383

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2003-01-23

Regulatory Status

Discontinued

2006
26 Dec
Discontinued Application: 77368

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-12-26

77368 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77368

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-12-26

Regulatory Status

Discontinued

2006
26 Dec
Discontinued Application: 77343

Drug Name

ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-12-26

77343 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

77343

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2006-12-26

Regulatory Status

Discontinued

2006
05 Dec
Discontinued Application: 77395

Drug Name

PAROXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

2006-12-05

77395 / 1

Active Ingredient

PAROXETINE HYDROCHLORIDE

Application Number

77395

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

2006-12-05

Regulatory Status

Discontinued

2006
26 Jan
Discontinued Application: 76240

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2006-01-26

76240 / 1

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

76240

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2006-01-26

Regulatory Status

Discontinued

2006
26 Jan
Discontinued Application: 76240

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-01-26

76240 / 2

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

76240

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-01-26

Regulatory Status

Discontinued

2006
26 Jan
Discontinued Application: 76240

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-01-26

76240 / 3

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

76240

Product Number

3

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2006-01-26

Regulatory Status

Discontinued

2006
26 Jan
Discontinued Application: 76240

Drug Name

QUINAPRIL HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-01-26

76240 / 4

Active Ingredient

QUINAPRIL HYDROCHLORIDE

Application Number

76240

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2006-01-26

Regulatory Status

Discontinued

2007
17 Sep
Discontinued Application: 77602

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/ML

Approval Date

2007-09-17

77602 / 1

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

77602

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/ML

Approval Date

2007-09-17

Regulatory Status

Discontinued

2012
31 May
Discontinued Application: 200172

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2012-05-31

200172 / 1

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

200172

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2012-05-31

Regulatory Status

Discontinued

2013
12 Sep
Discontinued Application: 201950

Drug Name

RASAGILINE MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5MG BASE

Approval Date

2013-09-12

201950 / 1

Active Ingredient

RASAGILINE MESYLATE

Application Number

201950

Product Number

1

Dosage Form

-

Strength

EQ 0.5MG BASE

Approval Date

2013-09-12

Regulatory Status

Discontinued

2013
12 Sep
Discontinued Application: 201950

Drug Name

RASAGILINE MESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2013-09-12

201950 / 2

Active Ingredient

RASAGILINE MESYLATE

Application Number

201950

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2013-09-12

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2008-09-15

77953 / 1

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2008-09-15

77953 / 2

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2008-09-15

77953 / 3

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2008-09-15

77953 / 4

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

5

Dosage Form

-

Strength

3MG

Approval Date

2008-09-15

77953 / 5

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

5

Dosage Form

-

Strength

3MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2008
15 Sep
Discontinued Application: 77953

Drug Name

RISPERIDONE

Product Number

6

Dosage Form

-

Strength

4MG

Approval Date

2008-09-15

77953 / 6

Active Ingredient

RISPERIDONE

Application Number

77953

Product Number

6

Dosage Form

-

Strength

4MG

Approval Date

2008-09-15

Regulatory Status

Discontinued

2013
16 May
Discontinued Application: 91072

Drug Name

RIVASTIGMINE TARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 1.5MG BASE

Approval Date

2013-05-16

91072 / 1

Active Ingredient

RIVASTIGMINE TARTRATE

Application Number

91072

Product Number

1

Dosage Form

-

Strength

EQ 1.5MG BASE

Approval Date

2013-05-16

Regulatory Status

Discontinued

2013
16 May
Discontinued Application: 91072

Drug Name

RIVASTIGMINE TARTRATE

Product Number

2

Dosage Form

-

Strength

EQ 3MG BASE

Approval Date

2013-05-16

91072 / 2

Active Ingredient

RIVASTIGMINE TARTRATE

Application Number

91072

Product Number

2

Dosage Form

-

Strength

EQ 3MG BASE

Approval Date

2013-05-16

Regulatory Status

Discontinued

2013
16 May
Discontinued Application: 91072

Drug Name

RIVASTIGMINE TARTRATE

Product Number

3

Dosage Form

-

Strength

EQ 4.5MG BASE

Approval Date

2013-05-16

91072 / 3

Active Ingredient

RIVASTIGMINE TARTRATE

Application Number

91072

Product Number

3

Dosage Form

-

Strength

EQ 4.5MG BASE

Approval Date

2013-05-16

Regulatory Status

Discontinued

2013
16 May
Discontinued Application: 91072

Drug Name

RIVASTIGMINE TARTRATE

Product Number

4

Dosage Form

-

Strength

EQ 6MG BASE

Approval Date

2013-05-16

91072 / 4

Active Ingredient

RIVASTIGMINE TARTRATE

Application Number

91072

Product Number

4

Dosage Form

-

Strength

EQ 6MG BASE

Approval Date

2013-05-16

Regulatory Status

Discontinued

2012
31 Dec
Discontinued Application: 202244

Drug Name

RIZATRIPTAN BENZOATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-12-31

202244 / 1

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

202244

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-12-31

Regulatory Status

Discontinued

2012
31 Dec
Discontinued Application: 202244

Drug Name

RIZATRIPTAN BENZOATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-12-31

202244 / 2

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

202244

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2012-12-31

Regulatory Status

Discontinued

2013
01 Jul
Discontinued Application: 202477

Drug Name

RIZATRIPTAN BENZOATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2013-07-01

202477 / 1

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

202477

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2013-07-01

Regulatory Status

Discontinued

2013
01 Jul
Discontinued Application: 202477

Drug Name

RIZATRIPTAN BENZOATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2013-07-01

202477 / 2

Active Ingredient

RIZATRIPTAN BENZOATE

Application Number

202477

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2013-07-01

Regulatory Status

Discontinued

2000
08 Sep
Discontinued Application: 75411

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 0.25% BASE

Approval Date

2000-09-08

75411 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

75411

Product Number

1

Dosage Form

-

Strength

EQ 0.25% BASE

Approval Date

2000-09-08

Regulatory Status

Discontinued

2000
08 Sep
Discontinued Application: 75412

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2000-09-08

75412 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

75412

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2000-09-08

Regulatory Status

Discontinued

2002
25 Feb
Discontinued Application: 65087

Drug Name

TOBRAMYCIN

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2002-02-25

65087 / 1

Active Ingredient

TOBRAMYCIN

Application Number

65087

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2002-02-25

Regulatory Status

Discontinued

2013
21 Mar
Discontinued Application: 203026

Drug Name

VALSARTAN AND HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

12.5MG;80MG

Approval Date

2013-03-21

203026 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; VALSARTAN

Application Number

203026

Product Number

1

Dosage Form

-

Strength

12.5MG;80MG

Approval Date

2013-03-21

Regulatory Status

Discontinued

2013
21 Mar
Discontinued Application: 203026

Drug Name

VALSARTAN AND HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

12.5MG;160MG

Approval Date

2013-03-21

203026 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; VALSARTAN

Application Number

203026

Product Number

2

Dosage Form

-

Strength

12.5MG;160MG

Approval Date

2013-03-21

Regulatory Status

Discontinued

2013
21 Mar
Discontinued Application: 203026

Drug Name

VALSARTAN AND HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

12.5MG;320MG

Approval Date

2013-03-21

203026 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; VALSARTAN

Application Number

203026

Product Number

3

Dosage Form

-

Strength

12.5MG;320MG

Approval Date

2013-03-21

Regulatory Status

Discontinued

2013
21 Mar
Discontinued Application: 203026

Drug Name

VALSARTAN AND HYDROCHLOROTHIAZIDE

Product Number

4

Dosage Form

-

Strength

25MG;160MG

Approval Date

2013-03-21

203026 / 4

Active Ingredient

HYDROCHLOROTHIAZIDE; VALSARTAN

Application Number

203026

Product Number

4

Dosage Form

-

Strength

25MG;160MG

Approval Date

2013-03-21

Regulatory Status

Discontinued

2013
21 Mar
Discontinued Application: 203026

Drug Name

VALSARTAN AND HYDROCHLOROTHIAZIDE

Product Number

5

Dosage Form

-

Strength

25MG;320MG

Approval Date

2013-03-21

203026 / 5

Active Ingredient

HYDROCHLOROTHIAZIDE; VALSARTAN

Application Number

203026

Product Number

5

Dosage Form

-

Strength

25MG;320MG

Approval Date

2013-03-21

Regulatory Status

Discontinued

2013
14 May
Discontinued Application: 202078

Drug Name

ZOLMITRIPTAN

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-05-14

202078 / 1

Active Ingredient

ZOLMITRIPTAN

Application Number

202078

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-05-14

Regulatory Status

Discontinued

2013
14 May
Discontinued Application: 202078

Drug Name

ZOLMITRIPTAN

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-05-14

202078 / 2

Active Ingredient

ZOLMITRIPTAN

Application Number

202078

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-05-14

Regulatory Status

Discontinued

2013
14 May
Discontinued Application: 202476

Drug Name

ZOLMITRIPTAN

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-05-14

202476 / 1

Active Ingredient

ZOLMITRIPTAN

Application Number

202476

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2013-05-14

Regulatory Status

Discontinued

2013
14 May
Discontinued Application: 202476

Drug Name

ZOLMITRIPTAN

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-05-14

202476 / 2

Active Ingredient

ZOLMITRIPTAN

Application Number

202476

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2013-05-14

Regulatory Status

Discontinued

2007
23 Apr
Discontinued Application: 77884

Drug Name

ZOLPIDEM TARTRATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-04-23

77884 / 1

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

77884

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-04-23

Regulatory Status

Discontinued

2007
23 Apr
Discontinued Application: 77884

Drug Name

ZOLPIDEM TARTRATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-04-23

77884 / 2

Active Ingredient

ZOLPIDEM TARTRATE

Application Number

77884

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-04-23

Regulatory Status

Discontinued

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Drug Status Breakdown
114 total
  • Discontinued
Official Source

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

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FDA Approved Drug Record Details Preview

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

Drug Name

ABACAVIR SULFATE

Application Number

201570

Product Number

1

Active Ingredient

ABACAVIR SULFATE

Dosage Form

-

Strength

EQ 300MG BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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