NDC 0409-3414 – Metoclopramide

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

Human Prescription Drug 1 recall

Product NDC0409-3414

Product details

Brand name
Metoclopramide
Generic name
Metoclopramide
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA073118
Marketed since
February 2, 2006
Listing expires
December 31, 2027
Pharmacologic class
Dopamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Metoclopramide →

Package NDC codes (1)

Package NDCDescriptionSince
0409-3414-1125 VIAL, SINGLE-DOSE in 1 TRAY (0409-3414-11) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-3414-21)Aug 26, 2024

Recalls mentioning this NDC

Other Metoclopramide products