E.E.S - 54569-0126-0 - (Erythromycin Ethylsuccinate)

Alphabetical Index


Drug Information of E.E.S

Product NDC: 54569-0126
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: 54569-0126
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050207
Marketing Category: NDA
Start Marketing Date: 20110418

Package Information of E.E.S

Package NDC: 54569-0126-0
Package Description: 100 mL in 1 BOTTLE (54569-0126-0)

NDC Information of E.E.S

NDC Code 54569-0126-0
Proprietary Name E.E.S
Package Description 100 mL in 1 BOTTLE (54569-0126-0)
Product NDC 54569-0126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin Ethylsuccinate
Dosage Form Name GRANULE, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20110418
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
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