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Azithromycin - 54868-5648-2 - (azithromycin monohydrate)

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Drug Information of Azithromycin

Product NDC: 54868-5648
Proprietary Name: Azithromycin
Non Proprietary Name: azithromycin monohydrate
Active Ingredient(s): 200    mg/5mL & nbsp;   azithromycin monohydrate
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 54868-5648
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA050710
Marketing Category: ANDA
Start Marketing Date: 20060803

Package Information of Azithromycin

Package NDC: 54868-5648-2
Package Description: 15 mL in 1 BOTTLE (54868-5648-2)

NDC Information of Azithromycin

NDC Code 54868-5648-2
Proprietary Name Azithromycin
Package Description 15 mL in 1 BOTTLE (54868-5648-2)
Product NDC 54868-5648
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin monohydrate
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20060803
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AZITHROMYCIN
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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