Eptifibatide

Product NDC

59651-013

11-digit product format

596510013

Labeler code

59651

Product ID

59651-013_1de8006b-6b11-46a8-b8e8-c6c07b9c9555

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Eptifibatide

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

Aurobindo Pharma Limited

Application

ANDA206127

Marketing category

ANDA

Marketing start

2015-12-08

Marketing end

0000-00-00

Substance

EPTIFIBATIDE

Active strength

20 mg/10mL

Pharmacologic classes

Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record