NDC 0703-4502 – Metoclopramide

Metoclopramide Hydrochloride 5 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 4 recalls

Product NDC0703-4502

Product details

Brand name
Metoclopramide
Generic name
Metoclopramide
Labeler
Teva Parenteral Medicines, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA073135
Marketed since
September 4, 2024
Listing expires
December 31, 2027
Pharmacologic class
Dopamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Metoclopramide →

Package NDC codes (2)

Package NDCDescriptionSince
0703-4502-0425 VIAL, SINGLE-USE in 1 TRAY (0703-4502-04) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-01)Dec 1, 1991
0703-4502-9310 VIAL, SINGLE-USE in 1 CARTON (0703-4502-93) / 2 mL in 1 VIAL, SINGLE-USE (0703-4502-91)Sep 4, 2024

Recalls mentioning this NDC

Other Metoclopramide products