Home > National Drug Code (NDC) > Azithromycin

Azithromycin - 0781-1496-31 - (Azithromycin)

Alphabetical Index


Drug Information of Azithromycin

Product NDC: 0781-1496
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: 0781-1496
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065211
Marketing Category: ANDA
Start Marketing Date: 20051114

Package Information of Azithromycin

Package NDC: 0781-1496-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-1496-31)

NDC Information of Azithromycin

NDC Code 0781-1496-31
Proprietary Name Azithromycin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0781-1496-31)
Product NDC 0781-1496
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051114
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


General Information