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clarithromycin - 62037-777-05 - (clarithromycin)

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Drug Information of clarithromycin

Product NDC: 62037-777
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: 62037-777
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065145
Marketing Category: ANDA
Start Marketing Date: 20080101

Package Information of clarithromycin

Package NDC: 62037-777-05
Package Description: 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-777-05)

NDC Information of clarithromycin

NDC Code 62037-777-05
Proprietary Name clarithromycin
Package Description 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-777-05)
Product NDC 62037-777
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clarithromycin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name ANDA
Labeler Name Watson Pharma, 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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