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Azithromycin - 54868-5487-2 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 54868-5487
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: 54868-5487
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065212
Marketing Category: ANDA
Start Marketing Date: 20070810

Package Information of Azithromycin

Package NDC: 54868-5487-2
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (54868-5487-2)

NDC Information of Azithromycin

NDC Code 54868-5487-2
Proprietary Name Azithromycin
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (54868-5487-2)
Product NDC 54868-5487
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070810
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AZITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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