Irinotecan Hydrochloride

Product NDC

16714-725

11-digit product format

167140725

Labeler code

16714

Product ID

16714-725_44473c63-a13e-4fbc-b4b7-eb4ea1a48a31

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Irinotecan Hydrochloride

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

NorthStar RxLLC

Application

ANDA077219

Marketing category

ANDA

Marketing start

2017-06-15

Marketing end

0000-00-00

Substance

IRINOTECAN HYDROCHLORIDE

Active strength

20 mg/mL

Pharmacologic classes

Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record