Nesher Pharmaceuticals USA LLC
FDA Approved Drugs

Nesher Pharmaceuticals USA LLC

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 69
  • Latest Approval Date Nov 22, 2021
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Nesher Pharmaceuticals USA LLC

Country

U.S.A

Website

Visit Website

Email

info@nesher.com

Social Profiles

Company Snapshot

Nesher Pharmaceuticals USA LLC

13910 Saint Charles Rock Road Bridgeton MO 63044 USA

U.S.A

www.nesher.com/ info@nesher.com View on Map
FDA Approved Drug Records ( 69 records )
2007
31 Oct
Discontinued Application: 40795

Drug Name

BENZONATATE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-10-31

40795 / 1

Active Ingredient

BENZONATATE

Application Number

40795

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-10-31

Regulatory Status

Discontinued

2007
31 Oct
Discontinued Application: 40795

Drug Name

BENZONATATE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-10-31

40795 / 2

Active Ingredient

BENZONATATE

Application Number

40795

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-10-31

Regulatory Status

Discontinued

2002
27 Feb
Discontinued Application: 75572

Drug Name

BUSPIRONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-02-27

75572 / 1

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

75572

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-02-27

Regulatory Status

Discontinued

2002
27 Feb
Discontinued Application: 75572

Drug Name

BUSPIRONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2002-02-27

75572 / 2

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

75572

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2002-02-27

Regulatory Status

Discontinued

2002
27 Feb
Discontinued Application: 75572

Drug Name

BUSPIRONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2002-02-27

75572 / 3

Active Ingredient

BUSPIRONE HYDROCHLORIDE

Application Number

75572

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2002-02-27

Regulatory Status

Discontinued

2020
17 Jul
Discontinued Application: 211543

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

2020-07-17

211543 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

211543

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

2020-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2019-07-17

210080 / 1

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

1

Dosage Form

-

Strength

1.25MG;1.25MG;1.25MG;1.25MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2019-07-17

210080 / 2

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

2

Dosage Form

-

Strength

2.5MG;2.5MG;2.5MG;2.5MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2019-07-17

210080 / 3

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

3

Dosage Form

-

Strength

3.75MG;3.75MG;3.75MG;3.75MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2019-07-17

210080 / 4

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

4

Dosage Form

-

Strength

5MG;5MG;5MG;5MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2019-07-17

210080 / 5

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

5

Dosage Form

-

Strength

6.25MG;6.25MG;6.25MG;6.25MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2019
17 Jul
Discontinued Application: 210080

Drug Name

DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2019-07-17

210080 / 6

Active Ingredient

AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

Application Number

210080

Product Number

6

Dosage Form

-

Strength

7.5MG;7.5MG;7.5MG;7.5MG

Approval Date

2019-07-17

Regulatory Status

Discontinued

2002
31 Oct
Discontinued Application: 40365

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-10-31

40365 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

40365

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2002-10-31

Regulatory Status

Discontinued

2002
31 Oct
Discontinued Application: 40367

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2002-10-31

40367 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

40367

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2002-10-31

Regulatory Status

Discontinued

2016
28 Mar
Discontinued Application: 206588

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-03-28

206588 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

206588

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-03-28

Regulatory Status

Discontinued

2016
28 Mar
Discontinued Application: 206588

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2016-03-28

206588 / 2

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

206588

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2016-03-28

Regulatory Status

Discontinued

2017
27 Jun
Discontinued Application: 209111

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2017-06-27

209111 / 1

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

209111

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2017-06-27

Regulatory Status

Discontinued

2017
27 Jun
Discontinued Application: 209111

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2017-06-27

209111 / 2

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

209111

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2017-06-27

Regulatory Status

Discontinued

2017
27 Jun
Discontinued Application: 209111

Drug Name

DEXTROAMPHETAMINE SULFATE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2017-06-27

209111 / 3

Active Ingredient

DEXTROAMPHETAMINE SULFATE

Application Number

209111

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2017-06-27

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

420MG

Approval Date

2006-09-12

76563 / 1

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

1

Dosage Form

-

Strength

420MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

120MG

Approval Date

2006-09-12

76563 / 2

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

2

Dosage Form

-

Strength

120MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2006-09-12

76563 / 3

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

3

Dosage Form

-

Strength

180MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

240MG

Approval Date

2006-09-12

76563 / 4

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

4

Dosage Form

-

Strength

240MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

300MG

Approval Date

2006-09-12

76563 / 5

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

5

Dosage Form

-

Strength

300MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

2006
12 Sep
Discontinued Application: 76563

Drug Name

DILTIAZEM HYDROCHLORIDE

Product Number

6

Dosage Form

-

Strength

360MG

Approval Date

2006-09-12

76563 / 6

Active Ingredient

DILTIAZEM HYDROCHLORIDE

Application Number

76563

Product Number

6

Dosage Form

-

Strength

360MG

Approval Date

2006-09-12

Regulatory Status

Discontinued

1987
15 Dec
Discontinued Application: 71200

Drug Name

DISOPYRAMIDE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1987-12-15

71200 / 1

Active Ingredient

DISOPYRAMIDE PHOSPHATE

Application Number

71200

Product Number

1

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1987-12-15

Regulatory Status

Discontinued

2000
18 Oct
Discontinued Application: 75609

Drug Name

DOXAZOSIN MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2000-10-18

75609 / 1

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75609

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2000-10-18

Regulatory Status

Discontinued

2000
18 Oct
Discontinued Application: 75609

Drug Name

DOXAZOSIN MESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2000-10-18

75609 / 2

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75609

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2000-10-18

Regulatory Status

Discontinued

2000
18 Oct
Discontinued Application: 75609

Drug Name

DOXAZOSIN MESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2000-10-18

75609 / 3

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75609

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2000-10-18

Regulatory Status

Discontinued

2000
18 Oct
Discontinued Application: 75609

Drug Name

DOXAZOSIN MESYLATE

Product Number

4

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2000-10-18

75609 / 4

Active Ingredient

DOXAZOSIN MESYLATE

Application Number

75609

Product Number

4

Dosage Form

-

Strength

EQ 8MG BASE

Approval Date

2000-10-18

Regulatory Status

Discontinued

2021
22 Nov
Discontinued Application: 208263

Drug Name

DOXYCYCLINE HYCLATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2021-11-22

208263 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

208263

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2021-11-22

Regulatory Status

Discontinued

2021
22 Nov
Discontinued Application: 208263

Drug Name

DOXYCYCLINE HYCLATE

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2021-11-22

208263 / 2

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

208263

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2021-11-22

Regulatory Status

Discontinued

2004
10 Sep
Discontinued Application: 76865

Drug Name

FLUTICASONE PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2004-09-10

76865 / 1

Active Ingredient

FLUTICASONE PROPIONATE

Application Number

76865

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2004-09-10

Regulatory Status

Discontinued

2002
23 Jan
Discontinued Application: 40366

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2002-01-23

40366 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40366

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2002-01-23

Regulatory Status

Discontinued

2005
09 Nov
Discontinued Application: 77311

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2005-11-09

77311 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

77311

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2005-11-09

Regulatory Status

Discontinued

2005
09 Nov
Discontinued Application: 77311

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2005-11-09

77311 / 2

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

77311

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2005-11-09

Regulatory Status

Discontinued

2005
09 Nov
Discontinued Application: 77311

Drug Name

HYDROMORPHONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

2005-11-09

77311 / 3

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

77311

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

2005-11-09

Regulatory Status

Discontinued

2007
18 May
Discontinued Application: 76640

Drug Name

METOPROLOL SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 200MG TARTRATE

Approval Date

2007-05-18

76640 / 1

Active Ingredient

METOPROLOL SUCCINATE

Application Number

76640

Product Number

1

Dosage Form

-

Strength

EQ 200MG TARTRATE

Approval Date

2007-05-18

Regulatory Status

Discontinued

2007
18 May
Discontinued Application: 76640

Drug Name

METOPROLOL SUCCINATE

Product Number

2

Dosage Form

-

Strength

EQ 100MG TARTRATE

Approval Date

2007-05-18

76640 / 2

Active Ingredient

METOPROLOL SUCCINATE

Application Number

76640

Product Number

2

Dosage Form

-

Strength

EQ 100MG TARTRATE

Approval Date

2007-05-18

Regulatory Status

Discontinued

2008
14 May
Discontinued Application: 77176

Drug Name

METOPROLOL SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 50MG TARTRATE

Approval Date

2008-05-14

77176 / 1

Active Ingredient

METOPROLOL SUCCINATE

Application Number

77176

Product Number

1

Dosage Form

-

Strength

EQ 50MG TARTRATE

Approval Date

2008-05-14

Regulatory Status

Discontinued

2008
20 Mar
Discontinued Application: 77779

Drug Name

METOPROLOL SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG TARTRATE

Approval Date

2008-03-20

77779 / 1

Active Ingredient

METOPROLOL SUCCINATE

Application Number

77779

Product Number

1

Dosage Form

-

Strength

EQ 25MG TARTRATE

Approval Date

2008-03-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18238

Drug Name

MICRO-K

Product Number

1

Dosage Form

-

Strength

8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

18238 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

18238

Product Number

1

Dosage Form

-

Strength

8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
14 May
Discontinued Application: 18238

Drug Name

MICRO-K 10

Product Number

2

Dosage Form

-

Strength

10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-05-14

18238 / 2

Active Ingredient

POTASSIUM CHLORIDE

Application Number

18238

Product Number

2

Dosage Form

-

Strength

10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-05-14

Regulatory Status

Discontinued

2004
19 May
Discontinued Application: 76720

Drug Name

MORPHINE SULFATE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2004-05-19

76720 / 1

Active Ingredient

MORPHINE SULFATE

Application Number

76720

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2004-05-19

Regulatory Status

Discontinued

2005
23 Dec
Discontinued Application: 76720

Drug Name

MORPHINE SULFATE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2005-12-23

76720 / 2

Active Ingredient

MORPHINE SULFATE

Application Number

76720

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

2005-12-23

Regulatory Status

Discontinued

2004
19 May
Discontinued Application: 76733

Drug Name

MORPHINE SULFATE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2004-05-19

76733 / 1

Active Ingredient

MORPHINE SULFATE

Application Number

76733

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

2004-05-19

Regulatory Status

Discontinued

2007
27 Sep
Discontinued Application: 77855

Drug Name

MORPHINE SULFATE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-09-27

77855 / 1

Active Ingredient

MORPHINE SULFATE

Application Number

77855

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2007-09-27

Regulatory Status

Discontinued

2007
27 Sep
Discontinued Application: 77855

Drug Name

MORPHINE SULFATE

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-09-27

77855 / 2

Active Ingredient

MORPHINE SULFATE

Application Number

77855

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2007-09-27

Regulatory Status

Discontinued

2006
18 Aug
Discontinued Application: 65321

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM

Approval Date

2006-08-18

65321 / 1

Active Ingredient

NYSTATIN

Application Number

65321

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM

Approval Date

2006-08-18

Regulatory Status

Discontinued

2007
25 Jun
Discontinued Application: 77717

Drug Name

ONDANSETRON

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

77717 / 1

Active Ingredient

ONDANSETRON

Application Number

77717

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2007
25 Jun
Discontinued Application: 77717

Drug Name

ONDANSETRON

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

77717 / 2

Active Ingredient

ONDANSETRON

Application Number

77717

Product Number

2

Dosage Form

-

Strength

8MG

Approval Date

2007-06-25

Regulatory Status

Discontinued

2017
28 Dec
Discontinued Application: 210079

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

325MG;2.5MG

Approval Date

2017-12-28

210079 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

210079

Product Number

1

Dosage Form

-

Strength

325MG;2.5MG

Approval Date

2017-12-28

Regulatory Status

Discontinued

2017
28 Dec
Discontinued Application: 210079

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

325MG;5MG

Approval Date

2017-12-28

210079 / 2

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

210079

Product Number

2

Dosage Form

-

Strength

325MG;5MG

Approval Date

2017-12-28

Regulatory Status

Discontinued

2017
28 Dec
Discontinued Application: 210079

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

325MG;7.5MG

Approval Date

2017-12-28

210079 / 3

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

210079

Product Number

3

Dosage Form

-

Strength

325MG;7.5MG

Approval Date

2017-12-28

Regulatory Status

Discontinued

2017
28 Dec
Discontinued Application: 210079

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

4

Dosage Form

-

Strength

325MG;10MG

Approval Date

2017-12-28

210079 / 4

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

210079

Product Number

4

Dosage Form

-

Strength

325MG;10MG

Approval Date

2017-12-28

Regulatory Status

Discontinued

2005
08 Dec
Discontinued Application: 77290

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2005-12-08

77290 / 1

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

77290

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2005-12-08

Regulatory Status

Discontinued

2005
08 Dec
Discontinued Application: 77290

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2005-12-08

77290 / 2

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

77290

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2005-12-08

Regulatory Status

Discontinued

2005
08 Dec
Discontinued Application: 77290

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2005-12-08

77290 / 3

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

77290

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2005-12-08

Regulatory Status

Discontinued

2005
08 Dec
Discontinued Application: 77290

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2005-12-08

77290 / 4

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

77290

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2005-12-08

Regulatory Status

Discontinued

2005
08 Dec
Discontinued Application: 77290

Drug Name

OXYCODONE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2005-12-08

77290 / 5

Active Ingredient

OXYCODONE HYDROCHLORIDE

Application Number

77290

Product Number

5

Dosage Form

-

Strength

30MG

Approval Date

2005-12-08

Regulatory Status

Discontinued

1987
17 Feb
Discontinued Application: 70980

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1987-02-17

70980 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

70980

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1987-02-17

Regulatory Status

Discontinued

2002
05 Apr
Discontinued Application: 76044

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

20MEQ

Approval Date

2002-04-05

76044 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

76044

Product Number

1

Dosage Form

-

Strength

20MEQ

Approval Date

2002-04-05

Regulatory Status

Discontinued

2002
10 Apr
Discontinued Application: 40364

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

15MG/5ML

Approval Date

2002-04-10

40364 / 1

Active Ingredient

PREDNISOLONE

Application Number

40364

Product Number

1

Dosage Form

-

Strength

15MG/5ML

Approval Date

2002-04-10

Regulatory Status

Discontinued

2001
22 Oct
Discontinued Application: 40423

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2001-10-22

40423 / 1

Active Ingredient

PREDNISOLONE

Application Number

40423

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2001-10-22

Regulatory Status

Discontinued

2005
24 May
Discontinued Application: 76982

Drug Name

PREDNISOLONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2005-05-24

76982 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

76982

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2005-05-24

Regulatory Status

Discontinued

2005
24 May
Discontinued Application: 76988

Drug Name

PREDNISOLONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/5ML

Approval Date

2005-05-24

76988 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

76988

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/5ML

Approval Date

2005-05-24

Regulatory Status

Discontinued

2002
07 Feb
Discontinued Application: 76193

Drug Name

PROPAFENONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2002-02-07

76193 / 1

Active Ingredient

PROPAFENONE HYDROCHLORIDE

Application Number

76193

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

2002-02-07

Regulatory Status

Discontinued

2002
07 Feb
Discontinued Application: 76193

Drug Name

PROPAFENONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

225MG

Approval Date

2002-02-07

76193 / 2

Active Ingredient

PROPAFENONE HYDROCHLORIDE

Application Number

76193

Product Number

2

Dosage Form

-

Strength

225MG

Approval Date

2002-02-07

Regulatory Status

Discontinued

2002
07 Feb
Discontinued Application: 76193

Drug Name

PROPAFENONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2002-02-07

76193 / 3

Active Ingredient

PROPAFENONE HYDROCHLORIDE

Application Number

76193

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2002-02-07

Regulatory Status

Discontinued

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Drug Status Breakdown
69 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

BENZONATATE

Application Number

40795

Product Number

1

Active Ingredient

BENZONATATE

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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Organized FDA drug records

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