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Azithromycin - 24236-906-38 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 24236-906
Proprietary Name: Azithromycin
Non Proprietary Name: Azithromycin
Active Ingredient(s): 500    mg/1 & nbsp;   Azithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin

Product NDC: 24236-906
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065405
Marketing Category: ANDA
Start Marketing Date: 20111115

Package Information of Azithromycin

Package NDC: 24236-906-38
Package Description: 3 TABLET in 1 BLISTER PACK (24236-906-38)

NDC Information of Azithromycin

NDC Code 24236-906-38
Proprietary Name Azithromycin
Package Description 3 TABLET in 1 BLISTER PACK (24236-906-38)
Product NDC 24236-906
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111115
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name AZITHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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