Integrilin (Merck Sharp & Dohme Corp.)


Welcome to the PulseAid listing for the Integrilin drug offered from Merck Sharp & Dohme Corp.. 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: Merck Sharp & Dohme Corp.
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: NDA
START MARKETING DATE: 2015-01-23
END MARKETING DATE: 0000-00-00


Integrilin HUMAN PRESCRIPTION DRUG Details:

Item DescriptionIntegrilin from Merck Sharp & Dohme Corp.
LABELER NAME: Merck Sharp & Dohme Corp.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.75(mg/mL)
START MARKETING DATE: 2015-01-23
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0085-1136_09400257-b29a-4eb6-972b-25b966979db5
PRODUCT NDC: 0085-1136
APPLICATION NUMBER: NDA020718

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