Carboplatin

Product NDC

66758-047

11-digit product format

667580047

Labeler code

66758

Product ID

66758-047_4ab1835d-95a1-4864-9739-d26fee1e4d8b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carboplatin

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA078280

Marketing category

ANDA

Marketing start

2010-01-31

Marketing end

0000-00-00

Substance

CARBOPLATIN

Active strength

10 mg/mL

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record