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Azithromycin - 35356-704-06 - (Azithromycin)

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Drug Information of Azithromycin

Product NDC: 35356-704
Proprietary Name: Azithromycin
Non Proprietary Name: Azithromycin
Active Ingredient(s): 250    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: 35356-704
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065211
Marketing Category: ANDA
Start Marketing Date: 20051114

Package Information of Azithromycin

Package NDC: 35356-704-06
Package Description: 6 TABLET, FILM COATED in 1 BLISTER PACK (35356-704-06)

NDC Information of Azithromycin

NDC Code 35356-704-06
Proprietary Name Azithromycin
Package Description 6 TABLET, FILM COATED in 1 BLISTER PACK (35356-704-06)
Product NDC 35356-704
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051114
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name AZITHROMYCIN MONOHYDRATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Azithromycin


General Information