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Azithromycin - 0093-7149-31 - (Azithromycin Monohydrate)

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Drug Information of Azithromycin

Product NDC: 0093-7149
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: 0093-7149
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065419
Marketing Category: ANDA
Start Marketing Date: 20080922

Package Information of Azithromycin

Package NDC: 0093-7149-31
Package Description: 30 mL in 1 BOTTLE (0093-7149-31)

NDC Information of Azithromycin

NDC Code 0093-7149-31
Proprietary Name Azithromycin
Package Description 30 mL in 1 BOTTLE (0093-7149-31)
Product NDC 0093-7149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin Monohydrate
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20080922
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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