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Azithromycin - 50268-099-13 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 50268-099
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: 50268-099
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065405
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Azithromycin

Package NDC: 50268-099-13
Package Description: 30 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (50268-099-13)

NDC Information of Azithromycin

NDC Code 50268-099-13
Proprietary Name Azithromycin
Package Description 30 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (50268-099-13)
Product NDC 50268-099
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name AvPAK
Substance Name AZITHROMYCIN ANHYDROUS
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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