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Clarithromycin - 49349-332-02 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 49349-332
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: 49349-332
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065144
Marketing Category: ANDA
Start Marketing Date: 20110627

Package Information of Clarithromycin

Package NDC: 49349-332-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-332-02)

NDC Information of Clarithromycin

NDC Code 49349-332-02
Proprietary Name Clarithromycin
Package Description 30 TABLET in 1 BLISTER PACK (49349-332-02)
Product NDC 49349-332
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110627
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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