Home > National Drug Code (NDC) > Clarithromycin

Clarithromycin - 68382-762-14 - (Clarithromycin)

Alphabetical Index


Drug Information of Clarithromycin

Product NDC: 68382-762
Proprietary Name: Clarithromycin
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 Clarithromycin

Product NDC: 68382-762
Labeler Name: Zydus Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050662
Marketing Category: NDA
Start Marketing Date: 19911031

Package Information of Clarithromycin

Package NDC: 68382-762-14
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (68382-762-14)

NDC Information of Clarithromycin

NDC Code 68382-762-14
Proprietary Name Clarithromycin
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (68382-762-14)
Product NDC 68382-762
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 Zydus Pharmaceuticals USA Inc
Substance Name CLARITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Clarithromycin


General Information