HALOPERIDOL

NDC 82619-107 · Creekwood Pharmaceuticals LLC

Generic namehaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength2 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

82619-107-01 — 100 TABLET in 1 BOTTLE (82619-107-01)

82619-107-02 — 1000 TABLET in 1 BOTTLE (82619-107-02)

FDA lists these products with the same active ingredient.

72162-2626 — haloperidol, 72205-064 — HALOPERIDOL, 72205-065 — HALOPERIDOL, 72205-066 — HALOPERIDOL, 72205-067 — HALOPERIDOL, 72205-068 — HALOPERIDOL, 72205-069 — HALOPERIDOL, 72789-558 — Haloperidol, 72789-559 — Haloperidol, 72789-566 — Haloperidol, 72789-567 — Haloperidol, 72789-568 — Haloperidol, 72789-569 — Haloperidol, 72888-173 — Haloperidol, 82619-105 — haloperidol, 82619-106 — haloperidol, 82619-108 — haloperidol, 82619-109 — haloperidol, 82619-110 — haloperidol, 87441-037 — Haloperidol, +136 more

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