Eptifibatide (Teva Parenteral Medicines, Inc.)


Welcome to the PulseAid listing for the Eptifibatide drug offered from Teva Parenteral Medicines, Inc.. This Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Teva Parenteral Medicines, Inc.
NON-PROPRIETARY NAME: Eptifibatide
SUBSTANCE NAME: EPTIFIBATIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2016-07-06
END MARKETING DATE: 0000-00-00


Eptifibatide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEptifibatide from Teva Parenteral Medicines, Inc.
LABELER NAME: Teva Parenteral Medicines, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 2(mg/mL)
START MARKETING DATE: 2016-07-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0703-1165_bd9c2668-0e91-44b2-8205-bdd8f82fa5c3
PRODUCT NDC: 0703-1165
APPLICATION NUMBER: ANDA090854

Other EPTIFIBATIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Akorn, Inc.Eptifibatide
Amneal BiosciencesEptifibatide
Aurobindo Pharma LimitedEptifibatide
AuroMedics Pharma LLCEptifibatide
Merck Sharp & Dohme Corp.Integrilin
Teva Parenteral Medicines, Inc.Eptifibatide