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Metoclopramide

NDC 0093-2204 · Teva Pharmaceuticals USA, Inc.

Generic nameMetoclopramide
Dosage formTABLET
RouteORAL
Active ingredient(s)METOCLOPRAMIDE HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classDopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

0093-2204-01 — 100 TABLET in 1 BOTTLE (0093-2204-01)

0093-2204-05 — 500 TABLET in 1 BOTTLE (0093-2204-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-2203 — Metoclopramide, 0121-0576 — metoclopramide hydrochloride, 0121-1576 — metoclopramide hydrochloride, 0404-9771 — metoclopramide hydrochloride, 0409-3414 — metoclopramide, 0409-5255 — metoclopramide, 0615-7698 — Metoclopramide, 0615-8285 — Metoclopramide, 0703-4502 — Metoclopramide, 17856-0576 — metoclopramide hydrochloride, 17856-1190 — Metoclopramide, 23155-240 — Metoclopramide Hydrochloride, 42291-596 — Metoclopramide, 43386-580 — Metoclopramide Hydrochloride, 43386-581 — Metoclopramide Hydrochloride, 48433-066 — Metoclopramide, 48433-067 — Metoclopramide, 50090-0132 — Metoclopramide, 50228-232 — Metoclopramide, 50228-233 — Metoclopramide, +56 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.