Vintage Pharmaceuticals-Charlotte Discontinued
FDA Approved Drugs

Vintage Pharmaceuticals-Charlotte 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 38
  • Latest Approval Date Jul 17, 2009
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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43
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Unclassified
5
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Discontinued
38
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Company Overview

Company

Vintage Pharmaceuticals-Charlotte Discontinued

Country

U.S.A

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Company Snapshot

Vintage Pharmaceuticals-Charlotte Discontinued

U.S.A

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FDA Approved Drug Records ( 38 records )
1982
01 Jan
Discontinued Application: 85409

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

85409 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

85409

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85410

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

85410 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

85410

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2003
25 Aug
Discontinued Application: 40513

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

500MG;50MG;40MG

Approval Date

2003-08-25

40513 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

40513

Product Number

1

Dosage Form

-

Strength

500MG;50MG;40MG

Approval Date

2003-08-25

Regulatory Status

Discontinued

1989
28 Jun
Discontinued Application: 62930

Drug Name

CLINDAMYCIN PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 1% BASE

Approval Date

1989-06-28

62930 / 1

Active Ingredient

CLINDAMYCIN PHOSPHATE

Application Number

62930

Product Number

1

Dosage Form

-

Strength

EQ 1% BASE

Approval Date

1989-06-28

Regulatory Status

Discontinued

1992
28 Jan
Discontinued Application: 73428

Drug Name

CO-LAV

Product Number

1

Dosage Form

-

Strength

240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

Approval Date

1992-01-28

73428 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Application Number

73428

Product Number

1

Dosage Form

-

Strength

240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

Approval Date

1992-01-28

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86296

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

86296 / 1

Active Ingredient

FOLIC ACID

Application Number

86296

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992
28 Apr
Discontinued Application: 73433

Drug Name

GO-EVAC

Product Number

1

Dosage Form

-

Strength

236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date

1992-04-28

73433 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Application Number

73433

Product Number

1

Dosage Form

-

Strength

236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date

1992-04-28

Regulatory Status

Discontinued

1996
22 Feb
Discontinued Application: 40143

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;10MG

Approval Date

1996-02-22

40143 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40143

Product Number

1

Dosage Form

-

Strength

650MG;10MG

Approval Date

1996-02-22

Regulatory Status

Discontinued

1996
22 Feb
Discontinued Application: 40144

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1996-02-22

40144 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40144

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1996-02-22

Regulatory Status

Discontinued

1997
25 Apr
Discontinued Application: 40144

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

1997-04-25

40144 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40144

Product Number

2

Dosage Form

-

Strength

500MG;2.5MG

Approval Date

1997-04-25

Regulatory Status

Discontinued

1997
14 Apr
Discontinued Application: 40155

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1997-04-14

40155 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40155

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1997-04-14

Regulatory Status

Discontinued

1996
12 Apr
Discontinued Application: 40157

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1996-04-12

40157 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40157

Product Number

1

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1996-04-12

Regulatory Status

Discontinued

1998
30 Sep
Discontinued Application: 40280

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1998-09-30

40280 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40280

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998
30 Sep
Discontinued Application: 40280

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1998-09-30

40280 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40280

Product Number

2

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998
30 Sep
Discontinued Application: 40280

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

650MG;10MG

Approval Date

1998-09-30

40280 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40280

Product Number

3

Dosage Form

-

Strength

650MG;10MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998
30 Sep
Discontinued Application: 40281

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1998-09-30

40281 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40281

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

1998
30 Sep
Discontinued Application: 40281

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1998-09-30

40281 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40281

Product Number

2

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1998-09-30

Regulatory Status

Discontinued

2000
31 May
Discontinued Application: 40356

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;10MG

Approval Date

2000-05-31

40356 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40356

Product Number

1

Dosage Form

-

Strength

500MG;10MG

Approval Date

2000-05-31

Regulatory Status

Discontinued

2000
31 May
Discontinued Application: 40358

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

660MG;10MG

Approval Date

2000-05-31

40358 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40358

Product Number

1

Dosage Form

-

Strength

660MG;10MG

Approval Date

2000-05-31

Regulatory Status

Discontinued

2003
30 Oct
Discontinued Application: 40520

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2003-10-30

40520 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40520

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2003-10-30

Regulatory Status

Discontinued

1988
07 Sep
Discontinued Application: 89831

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1988-09-07

89831 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89831

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1988-09-07

Regulatory Status

Discontinued

1988
02 Dec
Discontinued Application: 89971

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1988-12-02

89971 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89971

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1988-12-02

Regulatory Status

Discontinued

1996
30 Jul
Discontinued Application: 40106

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1996-07-30

40106 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40106

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1996-07-30

Regulatory Status

Discontinued

1999
30 Dec
Discontinued Application: 40303

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1999-12-30

40303 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40303

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1999-12-30

Regulatory Status

Discontinued

2000
19 Apr
Discontinued Application: 75328

Drug Name

PEMOLINE

Product Number

1

Dosage Form

-

Strength

18.75MG

Approval Date

2000-04-19

75328 / 1

Active Ingredient

PEMOLINE

Application Number

75328

Product Number

1

Dosage Form

-

Strength

18.75MG

Approval Date

2000-04-19

Regulatory Status

Discontinued

2000
19 Apr
Discontinued Application: 75328

Drug Name

PEMOLINE

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

2000-04-19

75328 / 2

Active Ingredient

PEMOLINE

Application Number

75328

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

2000-04-19

Regulatory Status

Discontinued

2000
19 Apr
Discontinued Application: 75328

Drug Name

PEMOLINE

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2000-04-19

75328 / 3

Active Ingredient

PEMOLINE

Application Number

75328

Product Number

3

Dosage Form

-

Strength

75MG

Approval Date

2000-04-19

Regulatory Status

Discontinued

1999
26 Jul
Discontinued Application: 40341

Drug Name

PERCOCET

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1999-07-26

40341 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40341

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1999-07-26

Regulatory Status

Discontinued

1999
26 Jul
Discontinued Application: 40341

Drug Name

PERCOCET

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

1999-07-26

40341 / 2

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40341

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

1999-07-26

Regulatory Status

Discontinued

2007
31 Oct
Discontinued Application: 78416

Drug Name

PREDNISOLONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2007-10-31

78416 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

78416

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE/5ML

Approval Date

2007-10-31

Regulatory Status

Discontinued

2009
17 Jul
Discontinued Application: 40908

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

2009-07-17

40908 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

40908

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

2009-07-17

Regulatory Status

Discontinued

2003
30 Jul
Discontinued Application: 40507

Drug Name

PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;65MG

Approval Date

2003-07-30

40507 / 1

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE

Application Number

40507

Product Number

1

Dosage Form

-

Strength

650MG;65MG

Approval Date

2003-07-30

Regulatory Status

Discontinued

1997
12 Feb
Discontinued Application: 74843

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1997-02-12

74843 / 1

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

74843

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

1997-02-12

Regulatory Status

Discontinued

2001
15 Feb
Discontinued Application: 74843

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

325MG;50MG

Approval Date

2001-02-15

74843 / 2

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

74843

Product Number

2

Dosage Form

-

Strength

325MG;50MG

Approval Date

2001-02-15

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83963

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

83963 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

83963

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
27 Nov
Discontinued Application: 40288

Drug Name

ZYDONE

Product Number

1

Dosage Form

-

Strength

400MG;5MG

Approval Date

1998-11-27

40288 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40288

Product Number

1

Dosage Form

-

Strength

400MG;5MG

Approval Date

1998-11-27

Regulatory Status

Discontinued

1998
27 Nov
Discontinued Application: 40288

Drug Name

ZYDONE

Product Number

2

Dosage Form

-

Strength

400MG;7.5MG

Approval Date

1998-11-27

40288 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40288

Product Number

2

Dosage Form

-

Strength

400MG;7.5MG

Approval Date

1998-11-27

Regulatory Status

Discontinued

1998
27 Nov
Discontinued Application: 40288

Drug Name

ZYDONE

Product Number

3

Dosage Form

-

Strength

400MG;10MG

Approval Date

1998-11-27

40288 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40288

Product Number

3

Dosage Form

-

Strength

400MG;10MG

Approval Date

1998-11-27

Regulatory Status

Discontinued

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Drug Status Breakdown
38 total
  • Discontinued
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

AMINOPHYLLINE

Application Number

85409

Product Number

1

Active Ingredient

AMINOPHYLLINE

Dosage Form

-

Strength

100MG

FDA Approved Drug Data

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