Ellence - 0009-5091-01 - (EPIRUBICIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of Ellence

Product NDC: 0009-5091
Proprietary Name: Ellence
Non Proprietary Name: EPIRUBICIN HYDROCHLORIDE
Active Ingredient(s): 2    mg/mL & nbsp;   EPIRUBICIN HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ellence

Product NDC: 0009-5091
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050778
Marketing Category: NDA
Start Marketing Date: 19990915

Package Information of Ellence

Package NDC: 0009-5091-01
Package Description: 25 mL in 1 VIAL, SINGLE-USE (0009-5091-01)

NDC Information of Ellence

NDC Code 0009-5091-01
Proprietary Name Ellence
Package Description 25 mL in 1 VIAL, SINGLE-USE (0009-5091-01)
Product NDC 0009-5091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPIRUBICIN HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19990915
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name EPIRUBICIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA]

Complete Information of Ellence


General Information