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AZITHROMYCIN - 50436-4356-1 - (AZITHROMYCIN)

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Drug Information of AZITHROMYCIN

Product NDC: 50436-4356
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: 50436-4356
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065404
Marketing Category: ANDA
Start Marketing Date: 20080211

Package Information of AZITHROMYCIN

Package NDC: 50436-4356-1
Package Description: 18 TABLET, FILM COATED in 1 BOTTLE (50436-4356-1)

NDC Information of AZITHROMYCIN

NDC Code 50436-4356-1
Proprietary Name AZITHROMYCIN
Package Description 18 TABLET, FILM COATED in 1 BOTTLE (50436-4356-1)
Product NDC 50436-4356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZITHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080211
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name AZITHROMYCIN ANHYDROUS
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of AZITHROMYCIN


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