Biaxin - 0074-3368-11 - (Clarithromycin)

Alphabetical Index


Drug Information of Biaxin

Product NDC: 0074-3368
Proprietary Name: Biaxin
Non Proprietary Name: Clarithromycin
Active Ingredient(s): 250    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: 0074-3368
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: 0074-3368-11
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-3368-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Biaxin

NDC Code 0074-3368-11
Proprietary Name Biaxin
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-3368-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0074-3368
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 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Biaxin


General Information