Alprazolam - 68788-9953-2 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 68788-9953
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: 68788-9953
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078491
Marketing Category: ANDA
Start Marketing Date: 20120112

Package Information of Alprazolam

Package NDC: 68788-9953-2
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (68788-9953-2)

NDC Information of Alprazolam

NDC Code 68788-9953-2
Proprietary Name Alprazolam
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (68788-9953-2)
Product NDC 68788-9953
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120112
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information