Alprazolam - 67046-963-30 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 67046-963
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: 67046-963
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19811016

Package Information of Alprazolam

Package NDC: 67046-963-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-963-30)

NDC Information of Alprazolam

NDC Code 67046-963-30
Proprietary Name Alprazolam
Package Description 30 TABLET in 1 BLISTER PACK (67046-963-30)
Product NDC 67046-963
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19811016
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Contract Pharmacy Services-PA
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information