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Azithromycin - 25021-112-10 - (azithromycin monohydrate)

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Drug Information of Azithromycin

Product NDC: 25021-112
Proprietary Name: Azithromycin
Non Proprietary Name: azithromycin monohydrate
Active Ingredient(s): 500    mg/5mL & nbsp;   azithromycin monohydrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 25021-112
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065506
Marketing Category: ANDA
Start Marketing Date: 20090501

Package Information of Azithromycin

Package NDC: 25021-112-10
Package Description: 10 VIAL in 1 CARTON (25021-112-10) > 5 mL in 1 VIAL

NDC Information of Azithromycin

NDC Code 25021-112-10
Proprietary Name Azithromycin
Package Description 10 VIAL in 1 CARTON (25021-112-10) > 5 mL in 1 VIAL
Product NDC 25021-112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin monohydrate
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090501
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 500
Strength Unit mg/5mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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