Haloperidol

NDC 59651-789 · Aurobindo Pharma Limited

Generic nameHaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength.5 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

59651-789-01 — 100 TABLET in 1 BOTTLE (59651-789-01)

59651-789-99 — 1000 TABLET in 1 BOTTLE (59651-789-99)

FDA lists these products with the same active ingredient.

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, 59651-790 — Haloperidol, 59651-791 — Haloperidol, 59651-792 — Haloperidol, 59651-793 — Haloperidol, 59651-794 — Haloperidol, 60687-161 — Haloperidol, 60687-799 — Haloperidol, 63629-2326 — Haloperidol, 63629-9270 — Haloperidol, 63629-9271 — 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.