CARBOPLATIN

Product NDC

47781-604

11-digit product format

477810604

Labeler code

47781

Product ID

47781-604_f5c03918-53f0-8acd-081f-21055276564a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carboplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Alvogen Inc.

Application

ANDA207324

Marketing category

ANDA

Marketing start

2018-02-01

Marketing end

2019-09-01

Substance

CARBOPLATIN

Active strength

10 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record