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azithromycin - 35356-798-03 - (azithromycin)

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Drug Information of azithromycin

Product NDC: 35356-798
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: 35356-798
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050784
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20020524

Package Information of azithromycin

Package NDC: 35356-798-03
Package Description: 3 TABLET, FILM COATED in 1 BLISTER PACK (35356-798-03)

NDC Information of azithromycin

NDC Code 35356-798-03
Proprietary Name azithromycin
Package Description 3 TABLET, FILM COATED in 1 BLISTER PACK (35356-798-03)
Product NDC 35356-798
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020524
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name AZITHROMYCIN ANHYDROUS
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of azithromycin


General Information