Alprazolam - 54569-3756-4 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 54569-3756
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): .5    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 54569-3756
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078491
Marketing Category: ANDA
Start Marketing Date: 20080925

Package Information of Alprazolam

Package NDC: 54569-3756-4
Package Description: 45 TABLET in 1 BOTTLE, PLASTIC (54569-3756-4)

NDC Information of Alprazolam

NDC Code 54569-3756-4
Proprietary Name Alprazolam
Package Description 45 TABLET in 1 BOTTLE, PLASTIC (54569-3756-4)
Product NDC 54569-3756
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080925
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information