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Azithromycin - 0093-7169-93 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 0093-7169
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: 0093-7169
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065193
Marketing Category: ANDA
Start Marketing Date: 20051116

Package Information of Azithromycin

Package NDC: 0093-7169-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-7169-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7169-19)

NDC Information of Azithromycin

NDC Code 0093-7169-93
Proprietary Name Azithromycin
Package Description 100 BLISTER PACK in 1 BOX (0093-7169-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7169-19)
Product NDC 0093-7169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051116
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


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