IXEMPRA - 0015-1911-13 - (ixabepilone)

Alphabetical Index


Drug Information of IXEMPRA

Product NDC: 0015-1911
Proprietary Name: IXEMPRA
Non Proprietary Name: ixabepilone
Active Ingredient(s):    & nbsp;   ixabepilone
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of IXEMPRA

Product NDC: 0015-1911
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022065
Marketing Category: NDA
Start Marketing Date: 20071016

Package Information of IXEMPRA

Package NDC: 0015-1911-13
Package Description: 1 KIT in 1 PACKAGE, COMBINATION (0015-1911-13) * 23.5 mL in 1 VIAL, SINGLE-USE * 23.5 mL in 1 VIAL, SINGLE-USE

NDC Information of IXEMPRA

NDC Code 0015-1911-13
Proprietary Name IXEMPRA
Package Description 1 KIT in 1 PACKAGE, COMBINATION (0015-1911-13) * 23.5 mL in 1 VIAL, SINGLE-USE * 23.5 mL in 1 VIAL, SINGLE-USE
Product NDC 0015-1911
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ixabepilone
Dosage Form Name KIT
Route Name
Start Marketing Date 20071016
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of IXEMPRA


General Information