NDC 71335-0362 – Metoclopramide

Metoclopramide Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0362

Product details

Brand name
Metoclopramide
Generic name
Metoclopramide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070184
Marketed since
September 30, 1990
Listing expires
December 31, 2026
Pharmacologic class
Dopamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Metoclopramide →

Package NDC codes (6)

Package NDCDescriptionSince
71335-0362-130 TABLET in 1 BOTTLE (71335-0362-1)Sep 6, 2018
71335-0362-290 TABLET in 1 BOTTLE (71335-0362-2)Dec 29, 2021
71335-0362-360 TABLET in 1 BOTTLE (71335-0362-3)Dec 29, 2021
71335-0362-410 TABLET in 1 BOTTLE (71335-0362-4)Dec 29, 2021
71335-0362-520 TABLET in 1 BOTTLE (71335-0362-5)Dec 29, 2021
71335-0362-6100 TABLET in 1 BOTTLE (71335-0362-6)Dec 29, 2021

Other Metoclopramide products