KENGREAL

Product NDC

65293-003

11-digit product format

652930003

Labeler code

65293

Product ID

65293-003_e16d2568-1d43-420c-a2b4-850f85861271

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cangrelor

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

The Medicines Company

Application

NDA204958

Marketing category

NDA

Marketing start

2015-07-08

Marketing end

0000-00-00

Substance

CANGRELOR

Active strength

50 mg/1

Pharmacologic classes

P2Y12 Platelet Inhibitor [EPC],Decreased Platelet Aggregation [PE],P2Y12 Receptor Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record