Oxaliplatin

Product NDC

51991-922

11-digit product format

519910922

Labeler code

51991

Product ID

51991-922_ef677720-77b1-433d-8c1d-121b7a55da55

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxaliplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA207325

Marketing category

ANDA

Marketing start

2017-02-20

Marketing end

2019-05-31

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