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METOCLOPRAMIDE hydrochloride

NDC 43386-580 · Lupin Pharmaceuticals,Inc.

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

Packages

43386-580-31 — 1 BLISTER PACK in 1 CARTON (43386-580-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 43386-581 — Metoclopramide Hydrochloride, 48433-066 — Metoclopramide, 48433-067 — Metoclopramide, 50090-0132 — Metoclopramide, 50228-232 — Metoclopramide, 50228-233 — Metoclopramide, 51079-886 — Metoclopramide, 51079-888 — Metoclopramide, 51655-240 — Metoclopramide, 51662-1288 — 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.