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Clarithromycin - 0093-7157-93 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 0093-7157
Proprietary Name: Clarithromycin
Non Proprietary Name: Clarithromycin
Active Ingredient(s): 250    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: 0093-7157
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065155
Marketing Category: ANDA
Start Marketing Date: 20050628

Package Information of Clarithromycin

Package NDC: 0093-7157-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-7157-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7157-19)

NDC Information of Clarithromycin

NDC Code 0093-7157-93
Proprietary Name Clarithromycin
Package Description 100 BLISTER PACK in 1 BOX (0093-7157-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7157-19)
Product NDC 0093-7157
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050628
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CLARITHROMYCIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Clarithromycin


General Information