Alprazolam - 0228-4022-11 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 0228-4022
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): .5    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 0228-4022
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078561
Marketing Category: ANDA
Start Marketing Date: 20100316

Package Information of Alprazolam

Package NDC: 0228-4022-11
Package Description: 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4022-11)

NDC Information of Alprazolam

NDC Code 0228-4022-11
Proprietary Name Alprazolam
Package Description 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0228-4022-11)
Product NDC 0228-4022
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20100316
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information