Alprazolam - 50436-4636-1 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 50436-4636
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 1    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 50436-4636
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074112
Marketing Category: ANDA
Start Marketing Date: 19951229

Package Information of Alprazolam

Package NDC: 50436-4636-1
Package Description: 30 TABLET in 1 BOTTLE (50436-4636-1)

NDC Information of Alprazolam

NDC Code 50436-4636-1
Proprietary Name Alprazolam
Package Description 30 TABLET in 1 BOTTLE (50436-4636-1)
Product NDC 50436-4636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19951229
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information