Alprazolam - 0904-5861-61 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 0904-5861
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 2    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 0904-5861
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074342
Marketing Category: ANDA
Start Marketing Date: 20080402

Package Information of Alprazolam

Package NDC: 0904-5861-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5861-61)

NDC Information of Alprazolam

NDC Code 0904-5861-61
Proprietary Name Alprazolam
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5861-61)
Product NDC 0904-5861
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080402
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ALPRAZOLAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information