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Azithromycin - 0093-2026-31 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 0093-2026
Proprietary Name: Azithromycin
Non Proprietary Name: Azithromycin
Active Ingredient(s): 200    mg/5mL & nbsp;   Azithromycin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 0093-2026
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065246
Marketing Category: ANDA
Start Marketing Date: 20101217

Package Information of Azithromycin

Package NDC: 0093-2026-31
Package Description: 30 mL in 1 BOTTLE (0093-2026-31)

NDC Information of Azithromycin

NDC Code 0093-2026-31
Proprietary Name Azithromycin
Package Description 30 mL in 1 BOTTLE (0093-2026-31)
Product NDC 0093-2026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20101217
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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