NDC 70436-162 – Eptifibatide

Eptifibatide 2 mg/mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC70436-162

Product details

Brand name
Eptifibatide
Generic name
eptifibatide
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA209864
Marketed since
June 1, 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
70436-162-8010 mL in 1 VIAL (70436-162-80)Dec 1, 2020

Recalls mentioning this NDC

Other Eptifibatide products