Alprazolam - 54868-2929-0 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 54868-2929
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): .25    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 54868-2929
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074046
Marketing Category: ANDA
Start Marketing Date: 20050317

Package Information of Alprazolam

Package NDC: 54868-2929-0
Package Description: 15 TABLET in 1 BOTTLE (54868-2929-0)

NDC Information of Alprazolam

NDC Code 54868-2929-0
Proprietary Name Alprazolam
Package Description 15 TABLET in 1 BOTTLE (54868-2929-0)
Product NDC 54868-2929
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050317
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information