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Clarithromycin - 64679-949-01 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 64679-949
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: 64679-949
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065266
Marketing Category: ANDA
Start Marketing Date: 20060531

Package Information of Clarithromycin

Package NDC: 64679-949-01
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (64679-949-01)

NDC Information of Clarithromycin

NDC Code 64679-949-01
Proprietary Name Clarithromycin
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (64679-949-01)
Product NDC 64679-949
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060531
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name CLARITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Clarithromycin


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