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AZITHROMYCIN - 68084-279-21 - (AZITHROMYCIN)

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Drug Information of AZITHROMYCIN

Product NDC: 68084-279
Proprietary Name: AZITHROMYCIN
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

Product NDC: 68084-279
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065404
Marketing Category: ANDA
Start Marketing Date: 20080402

Package Information of AZITHROMYCIN

Package NDC: 68084-279-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-279-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-279-11)

NDC Information of AZITHROMYCIN

NDC Code 68084-279-21
Proprietary Name AZITHROMYCIN
Package Description 3 BLISTER PACK in 1 CARTON (68084-279-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-279-11)
Product NDC 68084-279
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZITHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080402
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name AZITHROMYCIN ANHYDROUS
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of AZITHROMYCIN


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