E.E.S. - 55289-110-30 - (Erythromycin Ethylsuccinate)

Alphabetical Index


Drug Information of E.E.S.

Product NDC: 55289-110
Proprietary Name: E.E.S.
Non Proprietary Name: Erythromycin Ethylsuccinate
Active Ingredient(s): 400    mg/1 & nbsp;   Erythromycin Ethylsuccinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of E.E.S.

Product NDC: 55289-110
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061905
Marketing Category: ANDA
Start Marketing Date: 20101216

Package Information of E.E.S.

Package NDC: 55289-110-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-110-30)

NDC Information of E.E.S.

NDC Code 55289-110-30
Proprietary Name E.E.S.
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-110-30)
Product NDC 55289-110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin Ethylsuccinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101216
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ERYTHROMYCIN ETHYLSUCCINATE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of E.E.S.


General Information