Alprazolam - 0378-5024-91 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 0378-5024
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): 3    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: 0378-5024
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077391
Marketing Category: ANDA
Start Marketing Date: 20110504

Package Information of Alprazolam

Package NDC: 0378-5024-91
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-5024-91)

NDC Information of Alprazolam

NDC Code 0378-5024-91
Proprietary Name Alprazolam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-5024-91)
Product NDC 0378-5024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110504
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ALPRAZOLAM
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information