Eptifibatide

Product NDC

0703-1165

11-digit product format

007031165

Labeler code

0703

Product ID

0703-1165_41203614-4e19-4f14-8558-731acb9bb1ff

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Eptifibatide

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA090854

Marketing category

ANDA

Marketing start

2016-07-06

Marketing end

2019-05-31

Substance

EPTIFIBATIDE

Active strength

2 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record