Haloperidol

NDC 51079-735 · Mylan Institutional Inc.

Generic namehaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength2 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

51079-735-20 — 100 BLISTER PACK in 1 CARTON (51079-735-20) / 1 TABLET in 1 BLISTER PACK (51079-735-01)

FDA lists these products with the same active ingredient.

11788-072 — Haloperidol, 11788-073 — Haloperidol, 11788-074 — Haloperidol, 11788-075 — Haloperidol, 11788-076 — Haloperidol, 48433-151 — Haloperidol, 48433-152 — Haloperidol, 48433-153 — Haloperidol, 51079-733 — haloperidol, 51079-734 — haloperidol, 51079-736 — haloperidol, 55154-3566 — Haloperidol, 55154-5059 — haloperidol, 58657-700 — Haloperidol, 58657-701 — Haloperidol, 58657-702 — Haloperidol, 58657-703 — Haloperidol, 58657-704 — Haloperidol, 58657-705 — Haloperidol, 58657-900 — 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.