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azithromycin - 59762-3120-1 - (azithromycin)

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Drug Information of azithromycin

Product NDC: 59762-3120
Proprietary Name: azithromycin
Non Proprietary Name: azithromycin
Active Ingredient(s): 200    mg/5mL & nbsp;   azithromycin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of azithromycin

Product NDC: 59762-3120
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050710
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19951019

Package Information of azithromycin

Package NDC: 59762-3120-1
Package Description: 15 mL in 1 BOTTLE (59762-3120-1)

NDC Information of azithromycin

NDC Code 59762-3120-1
Proprietary Name azithromycin
Package Description 15 mL in 1 BOTTLE (59762-3120-1)
Product NDC 59762-3120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19951019
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name AZITHROMYCIN
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of azithromycin


General Information