ScieGen Pharmaceuticals Inc. Discontinued
FDA Approved Drugs

ScieGen Pharmaceuticals 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 37
  • Latest Approval Date Dec 10, 2024
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
266
View
Unclassified
6
View
Discontinued
37
View
OTC
4
View
RX
219
View
Company Overview

Company

ScieGen Pharmaceuticals Inc. Discontinued

Country

U.S.A

Website

Visit Website

Email

info@sciegenpharm.com

Social Profiles

Company Snapshot

ScieGen Pharmaceuticals Inc. Discontinued

20 Davids Driv, Hauppauge, NY 11788

U.S.A

sciegenpharm.com/ info@sciegenpharm.com View on Map
FDA Approved Drug Records ( 37 records )
2007
09 Jul
Discontinued Application: 77759

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-07-09

77759 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77759

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-07-09

Regulatory Status

Discontinued

2007
09 Jul
Discontinued Application: 77759

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-07-09

77759 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77759

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-07-09

Regulatory Status

Discontinued

2007
09 Jul
Discontinued Application: 77759

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-07-09

77759 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77759

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-07-09

Regulatory Status

Discontinued

2019
23 Aug
Discontinued Application: 210032

Drug Name

AZELASTINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.2055MG/SPRAY

Approval Date

2019-08-23

210032 / 1

Active Ingredient

AZELASTINE HYDROCHLORIDE

Application Number

210032

Product Number

1

Dosage Form

-

Strength

0.2055MG/SPRAY

Approval Date

2019-08-23

Regulatory Status

Discontinued

1995
30 Jan
Discontinued Application: 64028

Drug Name

BACITRACIN ZINC AND POLYMYXIN B SULFATE

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM;10,000 UNITS/GM

Approval Date

1995-01-30

64028 / 1

Active Ingredient

BACITRACIN ZINC; POLYMYXIN B SULFATE

Application Number

64028

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM;10,000 UNITS/GM

Approval Date

1995-01-30

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77316

Drug Name

CARVEDILOL

Product Number

1

Dosage Form

-

Strength

3.125MG

Approval Date

2007-09-05

77316 / 1

Active Ingredient

CARVEDILOL

Application Number

77316

Product Number

1

Dosage Form

-

Strength

3.125MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77316

Drug Name

CARVEDILOL

Product Number

2

Dosage Form

-

Strength

6.25MG

Approval Date

2007-09-05

77316 / 2

Active Ingredient

CARVEDILOL

Application Number

77316

Product Number

2

Dosage Form

-

Strength

6.25MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77316

Drug Name

CARVEDILOL

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2007-09-05

77316 / 3

Active Ingredient

CARVEDILOL

Application Number

77316

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

2007
05 Sep
Discontinued Application: 77316

Drug Name

CARVEDILOL

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

2007-09-05

77316 / 4

Active Ingredient

CARVEDILOL

Application Number

77316

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

2007-09-05

Regulatory Status

Discontinued

1996
07 May
Discontinued Application: 74356

Drug Name

CHLORHEXIDINE GLUCONATE

Product Number

1

Dosage Form

-

Strength

0.12%

Approval Date

1996-05-07

74356 / 1

Active Ingredient

CHLORHEXIDINE GLUCONATE

Application Number

74356

Product Number

1

Dosage Form

-

Strength

0.12%

Approval Date

1996-05-07

Regulatory Status

Discontinued

2017
28 Apr
Discontinued Application: 207218

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-04-28

207218 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

207218

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2017-04-28

Regulatory Status

Discontinued

1998
29 Apr
Discontinued Application: 74706

Drug Name

CROMOLYN SODIUM

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1998-04-29

74706 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

74706

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1998-04-29

Regulatory Status

Discontinued

2015
09 Dec
Discontinued Application: 205937

Drug Name

CYCLOPENTOLATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2015-12-09

205937 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

205937

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2015-12-09

Regulatory Status

Discontinued

2008
17 Apr
Discontinued Application: 77845

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-04-17

77845 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

77845

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2008-04-17

Regulatory Status

Discontinued

2015
24 Jul
Discontinued Application: 206572

Drug Name

DIFLORASONE DIACETATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2015-07-24

206572 / 1

Active Ingredient

DIFLORASONE DIACETATE

Application Number

206572

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2015-07-24

Regulatory Status

Discontinued

1990
28 Sep
Discontinued Application: 72416

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1990-09-28

72416 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

72416

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1990-09-28

Regulatory Status

Discontinued

2024
10 Dec
Discontinued Application: 211663

Drug Name

EZETIMIBE AND SIMVASTATIN

Product Number

1

Dosage Form

-

Strength

10MG;10MG

Approval Date

2024-12-10

211663 / 1

Active Ingredient

EZETIMIBE; SIMVASTATIN

Application Number

211663

Product Number

1

Dosage Form

-

Strength

10MG;10MG

Approval Date

2024-12-10

Regulatory Status

Discontinued

2024
10 Dec
Discontinued Application: 211663

Drug Name

EZETIMIBE AND SIMVASTATIN

Product Number

2

Dosage Form

-

Strength

10MG;20MG

Approval Date

2024-12-10

211663 / 2

Active Ingredient

EZETIMIBE; SIMVASTATIN

Application Number

211663

Product Number

2

Dosage Form

-

Strength

10MG;20MG

Approval Date

2024-12-10

Regulatory Status

Discontinued

2024
10 Dec
Discontinued Application: 211663

Drug Name

EZETIMIBE AND SIMVASTATIN

Product Number

3

Dosage Form

-

Strength

10MG;40MG

Approval Date

2024-12-10

211663 / 3

Active Ingredient

EZETIMIBE; SIMVASTATIN

Application Number

211663

Product Number

3

Dosage Form

-

Strength

10MG;40MG

Approval Date

2024-12-10

Regulatory Status

Discontinued

2024
10 Dec
Discontinued Application: 211663

Drug Name

EZETIMIBE AND SIMVASTATIN

Product Number

4

Dosage Form

-

Strength

10MG;80MG

Approval Date

2024-12-10

211663 / 4

Active Ingredient

EZETIMIBE; SIMVASTATIN

Application Number

211663

Product Number

4

Dosage Form

-

Strength

10MG;80MG

Approval Date

2024-12-10

Regulatory Status

Discontinued

2015
25 Jun
Discontinued Application: 91514

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2015-06-25

91514 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

91514

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2015-06-25

Regulatory Status

Discontinued

2016
09 Sep
Discontinued Application: 202705

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2016-09-09

202705 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

202705

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2016-09-09

Regulatory Status

Discontinued

1995
31 Aug
Discontinued Application: 64093

Drug Name

GENTAMICIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

1995-08-31

64093 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

64093

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

1995-08-31

Regulatory Status

Discontinued

2010
20 Dec
Discontinued Application: 90268

Drug Name

LEVOFLOXACIN

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2010-12-20

90268 / 1

Active Ingredient

LEVOFLOXACIN

Application Number

90268

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2010-12-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83244

Drug Name

NEMBUTAL

Product Number

1

Dosage Form

-

Strength

18.2MG/5ML

Approval Date

1982-01-01

83244 / 1

Active Ingredient

PENTOBARBITAL

Application Number

83244

Product Number

1

Dosage Form

-

Strength

18.2MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
25 Jan
Discontinued Application: 83247

Drug Name

NEMBUTAL

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-25

83247 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

83247

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

1982-01-25

Regulatory Status

Discontinued

1982
25 Jan
Discontinued Application: 83247

Drug Name

NEMBUTAL

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1982-01-25

83247 / 2

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

83247

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

1982-01-25

Regulatory Status

Discontinued

1982
25 Jan
Discontinued Application: 83247

Drug Name

NEMBUTAL

Product Number

3

Dosage Form

-

Strength

120MG

Approval Date

1982-01-25

83247 / 3

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

83247

Product Number

3

Dosage Form

-

Strength

120MG

Approval Date

1982-01-25

Regulatory Status

Discontinued

1982
25 Jan
Discontinued Application: 83247

Drug Name

NEMBUTAL

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

1982-01-25

83247 / 4

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

83247

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

1982-01-25

Regulatory Status

Discontinued

2004
06 Feb
Discontinued Application: 65088

Drug Name

NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

2004-02-06

65088 / 1

Active Ingredient

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

65088

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

2004-02-06

Regulatory Status

Discontinued

2012
25 Jul
Discontinued Application: 65213

Drug Name

NEOMYCIN AND POLYMYXIN B SULFATES, BACITRACIN ZINC AND HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

2012-07-25

65213 / 1

Active Ingredient

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

65213

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

2012-07-25

Regulatory Status

Discontinued

2017
10 Jan
Discontinued Application: 204532

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2017-01-10

204532 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

204532

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2017-01-10

Regulatory Status

Discontinued

2017
05 Dec
Discontinued Application: 204723

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2017-12-05

204723 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

204723

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2017-12-05

Regulatory Status

Discontinued

2022
14 Sep
Discontinued Application: 215675

Drug Name

PREGABALIN

Product Number

1

Dosage Form

-

Strength

82.5MG

Approval Date

2022-09-14

215675 / 1

Active Ingredient

PREGABALIN

Application Number

215675

Product Number

1

Dosage Form

-

Strength

82.5MG

Approval Date

2022-09-14

Regulatory Status

Discontinued

2022
14 Sep
Discontinued Application: 215675

Drug Name

PREGABALIN

Product Number

2

Dosage Form

-

Strength

165MG

Approval Date

2022-09-14

215675 / 2

Active Ingredient

PREGABALIN

Application Number

215675

Product Number

2

Dosage Form

-

Strength

165MG

Approval Date

2022-09-14

Regulatory Status

Discontinued

2022
14 Sep
Discontinued Application: 215675

Drug Name

PREGABALIN

Product Number

3

Dosage Form

-

Strength

330MG

Approval Date

2022-09-14

215675 / 3

Active Ingredient

PREGABALIN

Application Number

215675

Product Number

3

Dosage Form

-

Strength

330MG

Approval Date

2022-09-14

Regulatory Status

Discontinued

2016
11 Aug
Discontinued Application: 206312

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2016-08-11

206312 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

206312

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2016-08-11

Regulatory Status

Discontinued

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Drug Status Breakdown
37 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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Explore important FDA approved drug information available in the records above.

Drug Name

AMLODIPINE BESYLATE

Application Number

77759

Product Number

1

Active Ingredient

AMLODIPINE BESYLATE

Dosage Form

-

Strength

EQ 2.5MG BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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