NDC 55150-220 – Eptifibatide

Eptifibatide 200 mg/100mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC55150-220

Product details

Brand name
Eptifibatide
Generic name
Eptifibatide
Labeler
Eugia US LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA206127
Marketed since
December 8, 2015
Listing expires
December 31, 2026
Pharmacologic class
Platelet Aggregation Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Eptifibatide →

Package NDC codes (1)

Package NDCDescriptionSince
55150-220-991 VIAL, SINGLE-DOSE in 1 CARTON (55150-220-99) / 100 mL in 1 VIAL, SINGLE-DOSEDec 8, 2015

Recalls mentioning this NDC

Other Eptifibatide products