Luitpold Pharmaceuticals, Inc.
FDA Approved Drugs

Luitpold Pharmaceuticals, Inc.

FDA Approved Drugs Database

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

RX Discontinued
  • Total Records 31
  • Latest Approval Date Dec 29, 2010
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
31
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Discontinued
30
View
RX
1
View
Company Overview

Company

Luitpold Pharmaceuticals, Inc.

Country

U.S.A

Website

Visit Website

Email

inquiry@luitpold.com

Social Profiles

Company Snapshot

Luitpold Pharmaceuticals, Inc.

One Luitpold Drive P.O. Box 9001 Shirley, NY 11967

U.S.A

www.luitpold.com/ inquiry@luitpold.com View on Map
FDA Approved Drug Records ( 31 records )
1987
01 Dec
RX Application: 71192

Drug Name

AMINOCAPROIC ACID

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1987-12-01

71192 / 1

Active Ingredient

AMINOCAPROIC ACID

Application Number

71192

Product Number

1

Dosage Form

-

Strength

250MG/ML

Approval Date

1987-12-01

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 87240

Drug Name

AMINOPHYLLINE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

87240 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

87240

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2010
29 Mar
Discontinued Application: 91152

Drug Name

BENZTROPINE MESYLATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2010-03-29

91152 / 1

Active Ingredient

BENZTROPINE MESYLATE

Application Number

91152

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2010-03-29

Regulatory Status

Discontinued

1988
26 Jul
Discontinued Application: 70891

Drug Name

BRETYLIUM TOSYLATE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1988-07-26

70891 / 1

Active Ingredient

BRETYLIUM TOSYLATE

Application Number

70891

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1988-07-26

Regulatory Status

Discontinued

1994
20 Dec
Discontinued Application: 74353

Drug Name

CIMETIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE/2ML

Approval Date

1994-12-20

74353 / 1

Active Ingredient

CIMETIDINE HYDROCHLORIDE

Application Number

74353

Product Number

1

Dosage Form

-

Strength

EQ 300MG BASE/2ML

Approval Date

1994-12-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80668

Drug Name

CYANOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

0.03MG/ML

Approval Date

1982-01-01

80668 / 1

Active Ingredient

CYANOCOBALAMIN

Application Number

80668

Product Number

1

Dosage Form

-

Strength

0.03MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
21 Jul
Discontinued Application: 87440

Drug Name

DEXAMETHASONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 4MG PHOSPHATE/ML

Approval Date

1982-07-21

87440 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE

Application Number

87440

Product Number

1

Dosage Form

-

Strength

EQ 4MG PHOSPHATE/ML

Approval Date

1982-07-21

Regulatory Status

Discontinued

1998
25 Jun
Discontinued Application: 74545

Drug Name

DOBUTAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE/ML

Approval Date

1998-06-25

74545 / 1

Active Ingredient

DOBUTAMINE HYDROCHLORIDE

Application Number

74545

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE/ML

Approval Date

1998-06-25

Regulatory Status

Discontinued

1988
24 Oct
Discontinued Application: 72335

Drug Name

DROPERIDOL

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1988-10-24

72335 / 1

Active Ingredient

DROPERIDOL

Application Number

72335

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1988-10-24

Regulatory Status

Discontinued

2009
22 Dec
Discontinued Application: 78867

Drug Name

ETOMIDATE

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

2009-12-22

78867 / 1

Active Ingredient

ETOMIDATE

Application Number

78867

Product Number

1

Dosage Form

-

Strength

2MG/ML

Approval Date

2009-12-22

Regulatory Status

Discontinued

2003
01 Dec
Discontinued Application: 76656

Drug Name

FENOLDOPAM MESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2003-12-01

76656 / 1

Active Ingredient

FENOLDOPAM MESYLATE

Application Number

76656

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/ML

Approval Date

2003-12-01

Regulatory Status

Discontinued

1985
09 Oct
Discontinued Application: 89063

Drug Name

HEPARIN LOCK FLUSH

Product Number

1

Dosage Form

-

Strength

10 UNITS/ML

Approval Date

1985-10-09

89063 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

89063

Product Number

1

Dosage Form

-

Strength

10 UNITS/ML

Approval Date

1985-10-09

Regulatory Status

Discontinued

1985
09 Oct
Discontinued Application: 89064

Drug Name

HEPARIN LOCK FLUSH

Product Number

1

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

1985-10-09

89064 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

89064

Product Number

1

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

1985-10-09

Regulatory Status

Discontinued

1983
31 Oct
Discontinued Application: 87452

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1983-10-31

87452 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

87452

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

1983-10-31

Regulatory Status

Discontinued

2010
11 Jan
Discontinued Application: 90240

Drug Name

IBUTILIDE FUMARATE

Product Number

1

Dosage Form

-

Strength

0.1MG/ML

Approval Date

2010-01-11

90240 / 1

Active Ingredient

IBUTILIDE FUMARATE

Application Number

90240

Product Number

1

Dosage Form

-

Strength

0.1MG/ML

Approval Date

2010-01-11

Regulatory Status

Discontinued

2008
14 Jan
Discontinued Application: 78145

Drug Name

KETOROLAC TROMETHAMINE

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

2008-01-14

78145 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

78145

Product Number

1

Dosage Form

-

Strength

15MG/ML

Approval Date

2008-01-14

Regulatory Status

Discontinued

2008
14 Jan
Discontinued Application: 78145

Drug Name

KETOROLAC TROMETHAMINE

Product Number

2

Dosage Form

-

Strength

30MG/ML

Approval Date

2008-01-14

78145 / 2

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

78145

Product Number

2

Dosage Form

-

Strength

30MG/ML

Approval Date

2008-01-14

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83198

Drug Name

LIDOCAINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

83198 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

83198

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
21 Jan
Discontinued Application: 87409

Drug Name

MANNITOL 25%

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML

Approval Date

1982-01-21

87409 / 1

Active Ingredient

MANNITOL

Application Number

87409

Product Number

1

Dosage Form

-

Strength

12.5GM/50ML

Approval Date

1982-01-21

Regulatory Status

Discontinued

2010
29 Dec
Discontinued Application: 91307

Drug Name

METOPROLOL TARTRATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2010-12-29

91307 / 1

Active Ingredient

METOPROLOL TARTRATE

Application Number

91307

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2010-12-29

Regulatory Status

Discontinued

1988
24 May
Discontinued Application: 71492

Drug Name

NITROGLYCERIN

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1988-05-24

71492 / 1

Active Ingredient

NITROGLYCERIN

Application Number

71492

Product Number

1

Dosage Form

-

Strength

5MG/ML

Approval Date

1988-05-24

Regulatory Status

Discontinued

2008
18 Nov
Discontinued Application: 79039

Drug Name

ONDANSETRON HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2008-11-18

79039 / 1

Active Ingredient

ONDANSETRON HYDROCHLORIDE

Application Number

79039

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

2008-11-18

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80671

Drug Name

PIPERAZINE CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

80671 / 1

Active Ingredient

PIPERAZINE CITRATE

Application Number

80671

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80221

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

80221 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

80221

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80736

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

80736 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

80736

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87584

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

87584 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

87584

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87585

Drug Name

POTASSIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

87585 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

87585

Product Number

1

Dosage Form

-

Strength

2MEQ/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80669

Drug Name

PYRIDOXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

80669 / 1

Active Ingredient

PYRIDOXINE HYDROCHLORIDE

Application Number

80669

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80667

Drug Name

THIAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

80667 / 1

Active Ingredient

THIAMINE HYDROCHLORIDE

Application Number

80667

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
12 Nov
Discontinued Application: 70225

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1985-11-12

70225 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70225

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1985-11-12

Regulatory Status

Discontinued

1985
12 Nov
Discontinued Application: 70617

Drug Name

VERAPAMIL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1985-11-12

70617 / 1

Active Ingredient

VERAPAMIL HYDROCHLORIDE

Application Number

70617

Product Number

1

Dosage Form

-

Strength

2.5MG/ML

Approval Date

1985-11-12

Regulatory Status

Discontinued

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Drug Status Breakdown
31 total
  • RX
  • 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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Drug Name

AMINOCAPROIC ACID

Application Number

71192

Product Number

1

Active Ingredient

AMINOCAPROIC ACID

Dosage Form

-

Strength

250MG/ML

FDA Approved Drug Data

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