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Azithromycin Dihydrate - 60505-2582-0 - (azithromycin)

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Drug Information of Azithromycin Dihydrate

Product NDC: 60505-2582
Proprietary Name: Azithromycin Dihydrate
Non Proprietary Name: azithromycin
Active Ingredient(s): 500    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: 60505-2582
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065509
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Azithromycin Dihydrate

Package NDC: 60505-2582-0
Package Description: 3 BLISTER PACK in 1 CARTON (60505-2582-0) > 3 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Azithromycin Dihydrate

NDC Code 60505-2582-0
Proprietary Name Azithromycin Dihydrate
Package Description 3 BLISTER PACK in 1 CARTON (60505-2582-0) > 3 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2582
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name AZITHROMYCIN DIHYDRATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin Dihydrate


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