Cisplatin

Product NDC

47781-609

11-digit product format

477810609

Labeler code

47781

Product ID

47781-609_59de2dc4-7d8f-65bc-fd6f-1ad643473771

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cisplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Alvogen Inc.

Application

ANDA207323

Marketing category

ANDA

Marketing start

2017-09-25

Marketing end

2020-03-01

Substance

CISPLATIN

Active strength

50 mg/50mL

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