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Clarithromycin - 51079-673-06 - (clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 51079-673
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: 51079-673
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065195
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of Clarithromycin

Package NDC: 51079-673-06
Package Description: 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-673-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-673-01)

NDC Information of Clarithromycin

NDC Code 51079-673-06
Proprietary Name Clarithromycin
Package Description 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-673-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-673-01)
Product NDC 51079-673
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111006
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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