Luitpold Pharmaceuticals, Inc. Discontinued
FDA Approved Drugs
Luitpold 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.
- Total Records 30
- Latest Approval Date Dec 29, 2010
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Luitpold Pharmaceuticals, Inc. Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
Luitpold Pharmaceuticals, Inc. Discontinued
One Luitpold Drive P.O. Box 9001 Shirley, NY 11967
U.S.A
www.luitpold.com/ inquiry@luitpold.com View on MapFDA Approved Drug Records ( 30 records )
Drug Name
AMINOPHYLLINE
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Active Ingredient
AMINOPHYLLINE
Application Number
87240
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BENZTROPINE MESYLATE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2010-03-29
Active Ingredient
BENZTROPINE MESYLATE
Application Number
91152
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2010-03-29
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1988-07-26
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
70891
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1988-07-26
Regulatory Status
Discontinued
Drug Name
CIMETIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 300MG BASE/2ML
Approval Date
1994-12-20
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
Drug Name
CYANOCOBALAMIN
Product Number
1
Dosage Form
-
Strength
0.03MG/ML
Approval Date
1982-01-01
Active Ingredient
CYANOCOBALAMIN
Application Number
80668
Product Number
1
Dosage Form
-
Strength
0.03MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXAMETHASONE SODIUM PHOSPHATE
Product Number
1
Dosage Form
-
Strength
EQ 4MG PHOSPHATE/ML
Approval Date
1982-07-21
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
Drug Name
DOBUTAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 12.5MG BASE/ML
Approval Date
1998-06-25
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
Drug Name
DROPERIDOL
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1988-10-24
Active Ingredient
DROPERIDOL
Application Number
72335
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1988-10-24
Regulatory Status
Discontinued
Drug Name
ETOMIDATE
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2009-12-22
Active Ingredient
ETOMIDATE
Application Number
78867
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2009-12-22
Regulatory Status
Discontinued
Drug Name
FENOLDOPAM MESYLATE
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
2003-12-01
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
Drug Name
HEPARIN LOCK FLUSH
Product Number
1
Dosage Form
-
Strength
10 UNITS/ML
Approval Date
1985-10-09
Active Ingredient
HEPARIN SODIUM
Application Number
89063
Product Number
1
Dosage Form
-
Strength
10 UNITS/ML
Approval Date
1985-10-09
Regulatory Status
Discontinued
Drug Name
HEPARIN LOCK FLUSH
Product Number
1
Dosage Form
-
Strength
100 UNITS/ML
Approval Date
1985-10-09
Active Ingredient
HEPARIN SODIUM
Application Number
89064
Product Number
1
Dosage Form
-
Strength
100 UNITS/ML
Approval Date
1985-10-09
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM
Product Number
1
Dosage Form
-
Strength
1,000 UNITS/ML
Approval Date
1983-10-31
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
Drug Name
IBUTILIDE FUMARATE
Product Number
1
Dosage Form
-
Strength
0.1MG/ML
Approval Date
2010-01-11
Active Ingredient
IBUTILIDE FUMARATE
Application Number
90240
Product Number
1
Dosage Form
-
Strength
0.1MG/ML
Approval Date
2010-01-11
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
1
Dosage Form
-
Strength
15MG/ML
Approval Date
2008-01-14
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
78145
Product Number
1
Dosage Form
-
Strength
15MG/ML
Approval Date
2008-01-14
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
2
Dosage Form
-
Strength
30MG/ML
Approval Date
2008-01-14
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
78145
Product Number
2
Dosage Form
-
Strength
30MG/ML
Approval Date
2008-01-14
Regulatory Status
Discontinued
Drug Name
LIDOCAINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1982-01-01
Active Ingredient
LIDOCAINE HYDROCHLORIDE
Application Number
83198
Product Number
1
Dosage Form
-
Strength
2%
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 25%
Product Number
1
Dosage Form
-
Strength
12.5GM/50ML
Approval Date
1982-01-21
Active Ingredient
MANNITOL
Application Number
87409
Product Number
1
Dosage Form
-
Strength
12.5GM/50ML
Approval Date
1982-01-21
Regulatory Status
Discontinued
Drug Name
METOPROLOL TARTRATE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2010-12-29
Active Ingredient
METOPROLOL TARTRATE
Application Number
91307
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2010-12-29
Regulatory Status
Discontinued
Drug Name
NITROGLYCERIN
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1988-05-24
Active Ingredient
NITROGLYCERIN
Application Number
71492
Product Number
1
Dosage Form
-
Strength
5MG/ML
Approval Date
1988-05-24
Regulatory Status
Discontinued
Drug Name
ONDANSETRON HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
2008-11-18
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
Drug Name
PIPERAZINE CITRATE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/5ML
Approval Date
1982-01-01
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
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
80221
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
80736
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
87584
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
87585
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PYRIDOXINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Active Ingredient
PYRIDOXINE HYDROCHLORIDE
Application Number
80669
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
THIAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Active Ingredient
THIAMINE HYDROCHLORIDE
Application Number
80667
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VERAPAMIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1985-11-12
Active Ingredient
VERAPAMIL HYDROCHLORIDE
Application Number
70225
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1985-11-12
Regulatory Status
Discontinued
Drug Name
VERAPAMIL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
2.5MG/ML
Approval Date
1985-11-12
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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FDA Approved Drugs Database
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Drug Status Breakdown
30 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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Drug Name
AMINOPHYLLINE
Application Number
87240
Product Number
1
Active Ingredient
AMINOPHYLLINE
Dosage Form
-
Strength
25MG/ML
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