Epirubicin Hydrochloride

Product NDC
0115-1675
11-digit product format
001151675
Labeler code
0115
Product ID
0115-1675_4f954c6a-221b-494c-aea7-1a8c1b65e424
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epirubicin Hydrochloride
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Impax Generics
Application
ANDA065445
Marketing category
ANDA
Marketing start
2016-09-21
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
0115-1675-72ML - Milliliter0115-16755ee9e77c-9f68-45ec-87de-8cf3445b82f012017-03-06
0115-1675-73ML - Milliliter0115-1675a6c30d54-f165-4b19-b1ac-f247f9e9370b12016-11-08