Xanax - 0009-0059-07 - (ALPRAZOLAM)

Alphabetical Index


Drug Information of Xanax

Product NDC: 0009-0059
Proprietary Name: Xanax
Non Proprietary Name: ALPRAZOLAM
Active Ingredient(s): 1    mg/1 & nbsp;   ALPRAZOLAM
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Xanax

Product NDC: 0009-0059
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021434
Marketing Category: NDA
Start Marketing Date: 20030117

Package Information of Xanax

Package NDC: 0009-0059-07
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0059-07)

NDC Information of Xanax

NDC Code 0009-0059-07
Proprietary Name Xanax
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0059-07)
Product NDC 0009-0059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALPRAZOLAM
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030117
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Xanax


General Information