Alprazolam - 21695-247-30 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 21695-247
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: 21695-247
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074112
Marketing Category: ANDA
Start Marketing Date: 19991229

Package Information of Alprazolam

Package NDC: 21695-247-30
Package Description: 30 TABLET in 1 BOTTLE (21695-247-30)

NDC Information of Alprazolam

NDC Code 21695-247-30
Proprietary Name Alprazolam
Package Description 30 TABLET in 1 BOTTLE (21695-247-30)
Product NDC 21695-247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19991229
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information