Alprazolam - 21695-605-60 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 21695-605
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 2    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: 21695-605
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078387
Marketing Category: ANDA
Start Marketing Date: 20091203

Package Information of Alprazolam

Package NDC: 21695-605-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-605-60)

NDC Information of Alprazolam

NDC Code 21695-605-60
Proprietary Name Alprazolam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-605-60)
Product NDC 21695-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091203
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name ALPRAZOLAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information