ELOXATIN

Product NDC

12516-0592

11-digit product format

125160592

Labeler code

12516

Product ID

12516-0592_4057b792-ee8b-46ad-a497-9691e43d362b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxaliplatin

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Aventis Pharma Ltd.

Application

NDA021759

Marketing category

NDA

Marketing start

2009-07-22

Marketing end

0000-00-00

Substance

OXALIPLATIN

Active strength

5 mg/mL

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record