Biaxin - 0074-2586-60 - (Clarithromycin)

Alphabetical Index


Drug Information of Biaxin

Product NDC: 0074-2586
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
Coding System: National Drug Codes(NDC)

Labeler Information of Biaxin

Product NDC: 0074-2586
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050662
Marketing Category: NDA
Start Marketing Date: 19911031

Package Information of Biaxin

Package NDC: 0074-2586-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (0074-2586-60)

NDC Information of Biaxin

NDC Code 0074-2586-60
Proprietary Name Biaxin
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (0074-2586-60)
Product NDC 0074-2586
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19911031
Marketing Category Name NDA
Labeler Name AbbVie 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