NDC 70436-027 – Eptifibatide

Eptifibatide .75 mg/mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC70436-027

Product details

Brand name
Eptifibatide
Generic name
Eptifibatide
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA209864
Marketed since
July 22, 2019
Listing expires
December 31, 2027
Pharmacologic class
Platelet Aggregation Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Eptifibatide →

Package NDC codes (1)

Package NDCDescriptionSince
70436-027-80100 mL in 1 VIAL (70436-027-80)Jul 22, 2019

Recalls mentioning this NDC

Other Eptifibatide products