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Metoclopramide

NDC 51079-888 · Mylan Institutional Inc.

Generic nameMetoclopramide
Dosage formTABLET
RouteORAL
Active ingredient(s)METOCLOPRAMIDE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classDopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

51079-888-20 — 100 BLISTER PACK in 1 CARTON (51079-888-20) / 1 TABLET in 1 BLISTER PACK (51079-888-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 51079-886 — Metoclopramide, 51655-240 — Metoclopramide, 51662-1288 — METOCLOPRAMIDE, 51662-1367 — METOCLOPRAMIDE, 51662-1670 — METOCLOPRAMIDE, 55154-0450 — Metoclopramide, 55154-2353 — METOCLOPRAMIDE, 55154-4383 — Metoclopramide, 55154-7832 — metoclopramide, 60687-620 — Metoclopramide, 60687-631 — 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.