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Azithromycin - 63739-575-09 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 63739-575
Proprietary Name: Azithromycin
Non Proprietary Name: Azithromycin
Active Ingredient(s): 250    mg/1 & nbsp;   Azithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 63739-575
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065211
Marketing Category: ANDA
Start Marketing Date: 20121026

Package Information of Azithromycin

Package NDC: 63739-575-09
Package Description: 5 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-575-09) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Azithromycin

NDC Code 63739-575-09
Proprietary Name Azithromycin
Package Description 5 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-575-09) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-575
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121026
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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