CARBOPLATIN

Product NDC

69097-243

11-digit product format

690970243

Labeler code

69097

Product ID

69097-243_819cc4ff-98c7-4664-911f-b87e00340e78

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CARBOPLATIN

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Cipla USA Inc.

Application

ANDA077861

Marketing category

ANDA

Marketing start

2007-01-18

Marketing end

0000-00-00

Substance

CARBOPLATIN

Active strength

600 mg/60mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record