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Clarithromycin - 0093-7244-06 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 0093-7244
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Clarithromycin

Product NDC: 0093-7244
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065154
Marketing Category: ANDA
Start Marketing Date: 20060623

Package Information of Clarithromycin

Package NDC: 0093-7244-06
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7244-06)

NDC Information of Clarithromycin

NDC Code 0093-7244-06
Proprietary Name Clarithromycin
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7244-06)
Product NDC 0093-7244
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060623
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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