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Azithromycin - 52125-539-17 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 52125-539
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: 52125-539
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065211
Marketing Category: ANDA
Start Marketing Date: 20130523

Package Information of Azithromycin

Package NDC: 52125-539-17
Package Description: 4 TABLET, FILM COATED in 1 VIAL (52125-539-17)

NDC Information of Azithromycin

NDC Code 52125-539-17
Proprietary Name Azithromycin
Package Description 4 TABLET, FILM COATED in 1 VIAL (52125-539-17)
Product NDC 52125-539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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