Alprazolam - 0781-1089-05 - (Alprazolam)

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Drug Information of Alprazolam

Product NDC: 0781-1089
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 2    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 0781-1089
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074909
Marketing Category: ANDA
Start Marketing Date: 19980325

Package Information of Alprazolam

Package NDC: 0781-1089-05
Package Description: 500 TABLET in 1 BOTTLE (0781-1089-05)

NDC Information of Alprazolam

NDC Code 0781-1089-05
Proprietary Name Alprazolam
Package Description 500 TABLET in 1 BOTTLE (0781-1089-05)
Product NDC 0781-1089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980325
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ALPRAZOLAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information