Oxaliplatin

Product NDC

45963-637

11-digit product format

459630637

Labeler code

45963

Product ID

45963-637_acdb5f78-2177-4843-b8e4-fef38502aeb0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxaliplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Actavis Pharma, Inc.

Application

ANDA204880

Marketing category

ANDA

Marketing start

2018-08-03

Marketing end

2020-02-29

Substance

OXALIPLATIN

Active strength

5 mg/mL

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