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azithromycin - 54868-5938-0 - (azithromycin)

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Drug Information of azithromycin

Product NDC: 54868-5938
Proprietary Name: azithromycin
Non Proprietary Name: azithromycin
Active Ingredient(s): 1    g/1 & nbsp;   azithromycin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of azithromycin

Product NDC: 54868-5938
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050693
Marketing Category: NDA
Start Marketing Date: 20080908

Package Information of azithromycin

Package NDC: 54868-5938-0
Package Description: 3 POWDER, FOR SUSPENSION in 1 BOX (54868-5938-0)

NDC Information of azithromycin

NDC Code 54868-5938-0
Proprietary Name azithromycin
Package Description 3 POWDER, FOR SUSPENSION in 1 BOX (54868-5938-0)
Product NDC 54868-5938
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20080908
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name AZITHROMYCIN DIHYDRATE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of azithromycin


General Information