Xanax - 54868-1251-0 - (alprazolam)

Alphabetical Index


Drug Information of Xanax

Product NDC: 54868-1251
Proprietary Name: Xanax
Non Proprietary Name: alprazolam
Active Ingredient(s): 1    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Xanax

Product NDC: 54868-1251
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA
Start Marketing Date: 20031031

Package Information of Xanax

Package NDC: 54868-1251-0
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-1251-0)

NDC Information of Xanax

NDC Code 54868-1251-0
Proprietary Name Xanax
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-1251-0)
Product NDC 54868-1251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031031
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Xanax


General Information