Biaxin - 0074-3188-13 - (Clarithromycin)

Alphabetical Index


Drug Information of Biaxin

Product NDC: 0074-3188
Proprietary Name: Biaxin
Non Proprietary Name: Clarithromycin
Active Ingredient(s): 250    mg/5mL & nbsp;   Clarithromycin
Administration Route(s): ORAL
Dosage Form(s): GRANULE, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Biaxin

Product NDC: 0074-3188
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050698
Marketing Category: NDA
Start Marketing Date: 19931223

Package Information of Biaxin

Package NDC: 0074-3188-13
Package Description: 100 mL in 1 BOTTLE (0074-3188-13)

NDC Information of Biaxin

NDC Code 0074-3188-13
Proprietary Name Biaxin
Package Description 100 mL in 1 BOTTLE (0074-3188-13)
Product NDC 0074-3188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name GRANULE, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19931223
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name CLARITHROMYCIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Biaxin


General Information