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azithromycin - 49349-070-14 - (azithromycin)

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Drug Information of azithromycin

Product NDC: 49349-070
Proprietary Name: azithromycin
Non Proprietary Name: azithromycin
Active Ingredient(s): 500    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: 49349-070
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050784
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130305

Package Information of azithromycin

Package NDC: 49349-070-14
Package Description: 30 TABLET, FILM COATED in 1 VIAL (49349-070-14)

NDC Information of azithromycin

NDC Code 49349-070-14
Proprietary Name azithromycin
Package Description 30 TABLET, FILM COATED in 1 VIAL (49349-070-14)
Product NDC 49349-070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130305
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name REMEDYREPACK INC.
Substance Name AZITHROMYCIN, UNSPECIFIED FORM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of azithromycin


General Information