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CLARITHROMYCIN - 0179-0021-88 - (CLARITHROMYCIN)

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Drug Information of CLARITHROMYCIN

Product NDC: 0179-0021
Proprietary Name: CLARITHROMYCIN
Non Proprietary Name: CLARITHROMYCIN
Active Ingredient(s): 500    mg/1 & nbsp;   CLARITHROMYCIN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CLARITHROMYCIN

Product NDC: 0179-0021
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050662
Marketing Category: NDA
Start Marketing Date: 20091001

Package Information of CLARITHROMYCIN

Package NDC: 0179-0021-88
Package Description: 720 TABLET in 1 BOTTLE (0179-0021-88)

NDC Information of CLARITHROMYCIN

NDC Code 0179-0021-88
Proprietary Name CLARITHROMYCIN
Package Description 720 TABLET in 1 BOTTLE (0179-0021-88)
Product NDC 0179-0021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CLARITHROMYCIN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091001
Marketing Category Name NDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name CLARITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of CLARITHROMYCIN


General Information