Home > National Drug Code (NDC) > ERYTHROMYCIN

ERYTHROMYCIN - 24338-120-13 - (Erythromycin)

Alphabetical Index


Drug Information of ERYTHROMYCIN

Product NDC: 24338-120
Proprietary Name: ERYTHROMYCIN
Non Proprietary Name: Erythromycin
Active Ingredient(s): 250    mg/1 & nbsp;   Erythromycin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of ERYTHROMYCIN

Product NDC: 24338-120
Labeler Name: Arbor Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062746
Marketing Category: ANDA
Start Marketing Date: 20120110

Package Information of ERYTHROMYCIN

Package NDC: 24338-120-13
Package Description: 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24338-120-13)

NDC Information of ERYTHROMYCIN

NDC Code 24338-120-13
Proprietary Name ERYTHROMYCIN
Package Description 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (24338-120-13)
Product NDC 24338-120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120110
Marketing Category Name ANDA
Labeler Name Arbor Pharmaceuticals, Inc.
Substance Name ERYTHROMYCIN
Strength Number 250
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