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azithromycin - 59762-3060-3 - (azithromycin)

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Drug Information of azithromycin

Product NDC: 59762-3060
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: 59762-3060
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050711
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19960718

Package Information of azithromycin

Package NDC: 59762-3060-3
Package Description: 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (59762-3060-3)

NDC Information of azithromycin

NDC Code 59762-3060-3
Proprietary Name azithromycin
Package Description 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (59762-3060-3)
Product NDC 59762-3060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19960718
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name AZITHROMYCIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of azithromycin


General Information