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Azithromycin - 54868-3648-0 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 54868-3648
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: 54868-3648
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065212
Marketing Category: ANDA
Start Marketing Date: 19950815

Package Information of Azithromycin

Package NDC: 54868-3648-0
Package Description: 1 DOSE PACK in 1 BOTTLE, DISPENSING (54868-3648-0) > 3 TABLET, FILM COATED in 1 DOSE PACK

NDC Information of Azithromycin

NDC Code 54868-3648-0
Proprietary Name Azithromycin
Package Description 1 DOSE PACK in 1 BOTTLE, DISPENSING (54868-3648-0) > 3 TABLET, FILM COATED in 1 DOSE PACK
Product NDC 54868-3648
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950815
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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