NDC 0121-1576 – Metoclopramide

Metoclopramide Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-1576

Product details

Brand name
Metoclopramide
Generic name
Metoclopramide hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA072744
Marketed since
June 1, 1991
Listing expires
December 31, 2026
Pharmacologic class
Dopamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Metoclopramide →

Package NDC codes (1)

Package NDCDescriptionSince
0121-1576-1010 TRAY in 1 CASE (0121-1576-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSEJun 1, 1991

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