E.E.S - 24338-136-10 - (Erythromycin Ethylsuccinate)

Alphabetical Index


Drug Information of E.E.S

Product NDC: 24338-136
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: 24338-136
Labeler Name: Arbor Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050207
Marketing Category: NDA
Start Marketing Date: 20110418

Package Information of E.E.S

Package NDC: 24338-136-10
Package Description: 200 mL in 1 BOTTLE (24338-136-10)

NDC Information of E.E.S

NDC Code 24338-136-10
Proprietary Name E.E.S
Package Description 200 mL in 1 BOTTLE (24338-136-10)
Product NDC 24338-136
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 Arbor Pharmaceuticals, Inc.
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