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Azithromycin Dihydrate - 60505-2583-3 - (azithromycin)

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Drug Information of Azithromycin Dihydrate

Product NDC: 60505-2583
Proprietary Name: Azithromycin Dihydrate
Non Proprietary Name: azithromycin
Active Ingredient(s): 600    mg/1 & nbsp;   azithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Azithromycin Dihydrate

Product NDC: 60505-2583
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065508
Marketing Category: ANDA
Start Marketing Date: 20110713

Package Information of Azithromycin Dihydrate

Package NDC: 60505-2583-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (60505-2583-3)

NDC Information of Azithromycin Dihydrate

NDC Code 60505-2583-3
Proprietary Name Azithromycin Dihydrate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (60505-2583-3)
Product NDC 60505-2583
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110713
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name AZITHROMYCIN DIHYDRATE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin Dihydrate


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