Haloperidol

NDC 69292-582 · Amici Pharmaceuticals, LLC

Generic nameHaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength1 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

69292-582-01 — 100 TABLET in 1 BOTTLE (69292-582-01)

FDA lists these products with the same active ingredient.

67046-1673 — Haloperidol, 68084-249 — Haloperidol, 68084-250 — Haloperidol, 68382-079 — Haloperidol, 68382-080 — Haloperidol, 68382-081 — Haloperidol, 68382-407 — Haloperidol, 68382-408 — Haloperidol, 68382-409 — Haloperidol, 69292-580 — Haloperidol, 69292-584 — Haloperidol, 69292-586 — Haloperidol, 69292-588 — Haloperidol, 69292-590 — Haloperidol, 70518-1182 — Haloperidol, 70518-1269 — Haloperidol, 70518-1599 — Haloperidol, 70518-2680 — Haloperidol, 70518-2682 — Haloperidol, 70518-2687 — 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.