Xanax - 54868-0522-5 - (alprazolam)

Alphabetical Index


Drug Information of Xanax

Product NDC: 54868-0522
Proprietary Name: Xanax
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 Xanax

Product NDC: 54868-0522
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA
Start Marketing Date: 19970204

Package Information of Xanax

Package NDC: 54868-0522-5
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-0522-5)

NDC Information of Xanax

NDC Code 54868-0522-5
Proprietary Name Xanax
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-0522-5)
Product NDC 54868-0522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970204
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALPRAZOLAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Xanax


General Information