Biaxin - 54868-4191-0 - (Clarithromycin)

Alphabetical Index


Drug Information of Biaxin

Product NDC: 54868-4191
Proprietary Name: Biaxin
Non Proprietary Name: Clarithromycin
Active Ingredient(s): 500    mg/1 & nbsp;   Clarithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Biaxin

Product NDC: 54868-4191
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050775
Marketing Category: NDA
Start Marketing Date: 20001103

Package Information of Biaxin

Package NDC: 54868-4191-0
Package Description: 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-4191-0)

NDC Information of Biaxin

NDC Code 54868-4191-0
Proprietary Name Biaxin
Package Description 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-4191-0)
Product NDC 54868-4191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20001103
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLARITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Biaxin


General Information