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Azithromycin - 50111-794-78 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 50111-794
Proprietary Name: Azithromycin
Non Proprietary Name: Azithromycin
Active Ingredient(s): 100    mg/mL & nbsp;   Azithromycin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 50111-794
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065265
Marketing Category: ANDA
Start Marketing Date: 20070817

Package Information of Azithromycin

Package NDC: 50111-794-78
Package Description: 10 VIAL, SINGLE-USE in 1 PACKAGE (50111-794-78) > 5 mL in 1 VIAL, SINGLE-USE

NDC Information of Azithromycin

NDC Code 50111-794-78
Proprietary Name Azithromycin
Package Description 10 VIAL, SINGLE-USE in 1 PACKAGE (50111-794-78) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC 50111-794
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070817
Marketing Category Name ANDA
Labeler Name Pliva Inc.
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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