ALPRAZOLAM - 52959-965-30 - (ALPRAZOLAM)

Alphabetical Index


Drug Information of ALPRAZOLAM

Product NDC: 52959-965
Proprietary Name: ALPRAZOLAM
Non Proprietary Name: ALPRAZOLAM
Active Ingredient(s): 1    mg/1 & nbsp;   ALPRAZOLAM
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ALPRAZOLAM

Product NDC: 52959-965
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077996
Marketing Category: ANDA
Start Marketing Date: 20070328

Package Information of ALPRAZOLAM

Package NDC: 52959-965-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (52959-965-30)

NDC Information of ALPRAZOLAM

NDC Code 52959-965-30
Proprietary Name ALPRAZOLAM
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (52959-965-30)
Product NDC 52959-965
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALPRAZOLAM
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070328
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of ALPRAZOLAM


General Information