Xanax - 0009-0029-01 - (ALPRAZOLAM)

Alphabetical Index


Drug Information of Xanax

Product NDC: 0009-0029
Proprietary Name: Xanax
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 Xanax

Product NDC: 0009-0029
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA
Start Marketing Date: 19811016

Package Information of Xanax

Package NDC: 0009-0029-01
Package Description: 100 TABLET in 1 BOTTLE (0009-0029-01)

NDC Information of Xanax

NDC Code 0009-0029-01
Proprietary Name Xanax
Package Description 100 TABLET in 1 BOTTLE (0009-0029-01)
Product NDC 0009-0029
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
Labeler Name Pharmacia and Upjohn Company
Substance Name ALPRAZOLAM
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Xanax


General Information