Alprazolam - 55154-2092-0 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 55154-2092
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): .5    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 55154-2092
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074112
Marketing Category: ANDA
Start Marketing Date: 20071203

Package Information of Alprazolam

Package NDC: 55154-2092-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2092-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Alprazolam

NDC Code 55154-2092-0
Proprietary Name Alprazolam
Package Description 10 BLISTER PACK in 1 BAG (55154-2092-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-2092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071203
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information