Epirubicin Hydrochloride

Product NDC
63323-151
11-digit product format
633230151
Labeler code
63323
Product ID
63323-151_873ef01e-d426-42c1-8062-260253255b09
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
epirubicin hydrochloride
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Fresenius Kabi USA, LLC
Application
ANDA065411
Marketing category
ANDA
Marketing start
2017-07-31
Marketing end
0000-00-00
Substance
EPIRUBICIN HYDROCHLORIDE
Active strength
2 mg/mL
Pharmacologic classes
Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [CS],Topoisomerase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63323-151-00ML - Milliliter63323-1518999ce88-6436-4d90-a333-ec40d9160dd512013-02-13
63323-151-25ML - Milliliter63323-151cd8cbf6d-fdc0-448e-9636-490727a6bebc12013-02-13