NDC 50228-232 – Metoclopramide

Metoclopramide Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50228-232

Product details

Brand name
Metoclopramide
Generic name
Metoclopramide
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072215
Marketed since
February 12, 2025
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
50228-232-01100 TABLET in 1 BOTTLE (50228-232-01)Feb 12, 2025
50228-232-05500 TABLET in 1 BOTTLE (50228-232-05)Feb 12, 2025

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