Haloperidol

NDC 58657-701 · Method Pharmaceuticals, LLC

Generic nameHaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength1 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

58657-701-01 — 100 TABLET in 1 BOTTLE (58657-701-01)

FDA lists these products with the same active ingredient.

48433-151 — Haloperidol, 48433-152 — Haloperidol, 48433-153 — Haloperidol, 51079-733 — haloperidol, 51079-734 — haloperidol, 51079-735 — haloperidol, 51079-736 — haloperidol, 55154-3566 — Haloperidol, 55154-5059 — haloperidol, 58657-700 — Haloperidol, 58657-702 — Haloperidol, 58657-703 — Haloperidol, 58657-704 — Haloperidol, 58657-705 — Haloperidol, 58657-900 — Haloperidol, 58657-901 — Haloperidol, 58657-902 — Haloperidol, 58657-903 — Haloperidol, 58657-904 — Haloperidol, 58657-905 — Haloperidol, +136 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.