Oxaliplatin

Product NDC

47781-592

11-digit product format

477810592

Labeler code

47781

Product ID

47781-592_df0727c2-62cb-7ad1-dca8-f6229a5a9ff7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxaliplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Alvogen Inc.

Application

ANDA207325

Marketing category

ANDA

Marketing start

2017-07-31

Marketing end

2019-12-01

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