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Clarithromycin - 49999-904-14 - (Clarithromycin)

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Drug Information of Clarithromycin

Product NDC: 49999-904
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: 49999-904
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065136
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of Clarithromycin

Package NDC: 49999-904-14
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-904-14)

NDC Information of Clarithromycin

NDC Code 49999-904-14
Proprietary Name Clarithromycin
Package Description 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-904-14)
Product NDC 49999-904
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clarithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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