E.E.S. - 0074-6369-02 - (Erythromycin Ethylsuccinate)

Alphabetical Index


Drug Information of E.E.S.

Product NDC: 0074-6369
Proprietary Name: E.E.S.
Non Proprietary Name: Erythromycin Ethylsuccinate
Active Ingredient(s): 200    mg/5mL & nbsp;   Erythromycin Ethylsuccinate
Administration Route(s): ORAL
Dosage Form(s): GRANULE, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of E.E.S.

Product NDC: 0074-6369
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050207
Marketing Category: NDA
Start Marketing Date: 20101210

Package Information of E.E.S.

Package NDC: 0074-6369-02
Package Description: 100 mL in 1 BOTTLE (0074-6369-02)

NDC Information of E.E.S.

NDC Code 0074-6369-02
Proprietary Name E.E.S.
Package Description 100 mL in 1 BOTTLE (0074-6369-02)
Product NDC 0074-6369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin Ethylsuccinate
Dosage Form Name GRANULE, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20101210
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name ERYTHROMYCIN ETHYLSUCCINATE
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of E.E.S.


General Information