Oxaliplatin

Product NDC

51991-218

11-digit product format

519910218

Labeler code

51991

Product ID

51991-218_9c95e367-df33-4151-9986-b7dfaee642b1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxaliplatin

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA204616

Marketing category

ANDA

Marketing start

2017-09-01

Marketing end

2020-10-31

Substance

OXALIPLATIN

Active strength

50 mg/10mL

Pharmacologic classes

Platinum-based Drug [EPC],Platinum-containing Compounds [EXT]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record