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Clarithromycin - 52125-331-04 - (clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 52125-331
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: 52125-331
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065195
Marketing Category: ANDA
Start Marketing Date: 20130509

Package Information of Clarithromycin

Package NDC: 52125-331-04
Package Description: 14 TABLET, FILM COATED in 1 VIAL (52125-331-04)

NDC Information of Clarithromycin

NDC Code 52125-331-04
Proprietary Name Clarithromycin
Package Description 14 TABLET, FILM COATED in 1 VIAL (52125-331-04)
Product NDC 52125-331
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130509
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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