VINORELBINE

Product NDC
61703-341
11-digit product format
617030341
Labeler code
61703
Product ID
61703-341_7133a031-8cfa-4c67-8c09-12711a45184a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
vinorelbine
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Hospira, Inc.
Application
ANDA076827
Marketing category
ANDA
Marketing start
2007-04-02
Marketing end
2019-05-31
Substance
VINORELBINE TARTRATE
Active strength
10 mg/mL
Pharmacologic classes
Vinca Alkaloid [EPC],Vinca Alkaloids [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61703-341-06ML - Milliliter61703-341c554761d-a8d5-4d4b-97c8-19966dfaf55912012-07-24
61703-341-09ML - Milliliter61703-341875d6708-0edb-401d-a493-f73f890d946812012-07-24