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Clarithromycin - 21695-557-10 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 21695-557
Proprietary Name: Clarithromycin
Non Proprietary Name: Clarithromycin
Active Ingredient(s): 250    mg/1 & nbsp;   Clarithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clarithromycin

Product NDC: 21695-557
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065144
Marketing Category: ANDA
Start Marketing Date: 20051018

Package Information of Clarithromycin

Package NDC: 21695-557-10
Package Description: 10 TABLET in 1 BOTTLE (21695-557-10)

NDC Information of Clarithromycin

NDC Code 21695-557-10
Proprietary Name Clarithromycin
Package Description 10 TABLET in 1 BOTTLE (21695-557-10)
Product NDC 21695-557
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051018
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name CLARITHROMYCIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Clarithromycin


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