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AZITHROMYCIN - 55648-964-05 - (AZITHROMYCIN)

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Drug Information of AZITHROMYCIN

Product NDC: 55648-964
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: 55648-964
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065405
Marketing Category: ANDA
Start Marketing Date: 20080211

Package Information of AZITHROMYCIN

Package NDC: 55648-964-05
Package Description: 3 BLISTER PACK in 1 CARTON (55648-964-05) > 3 TABLET, FILM COATED in 1 BLISTER PACK (55648-964-03)

NDC Information of AZITHROMYCIN

NDC Code 55648-964-05
Proprietary Name AZITHROMYCIN
Package Description 3 BLISTER PACK in 1 CARTON (55648-964-05) > 3 TABLET, FILM COATED in 1 BLISTER PACK (55648-964-03)
Product NDC 55648-964
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZITHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080211
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
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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