Home > National Drug Code (NDC) > Erythromycin

Erythromycin - 35356-827-30 - (Erythromycin)

Alphabetical Index


Drug Information of Erythromycin

Product NDC: 35356-827
Proprietary Name: Erythromycin
Non Proprietary Name: Erythromycin
Active Ingredient(s): 500    mg/1 & nbsp;   Erythromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Erythromycin

Product NDC: 35356-827
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061621
Marketing Category: ANDA
Start Marketing Date: 20110906

Package Information of Erythromycin

Package NDC: 35356-827-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (35356-827-30)

NDC Information of Erythromycin

NDC Code 35356-827-30
Proprietary Name Erythromycin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (35356-827-30)
Product NDC 35356-827
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110906
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name ERYTHROMYCIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Erythromycin


General Information