Haloperidol

NDC 65841-837 · Zydus Lifesciences Limited

Generic nameHaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength.5 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

65841-837-01 — 100 TABLET in 1 BOTTLE (65841-837-01)

65841-837-10 — 1000 TABLET in 1 BOTTLE (65841-837-10)

65841-837-77 — 10 BLISTER PACK in 1 CARTON (65841-837-77) / 10 TABLET in 1 BLISTER PACK (65841-837-30)

FDA lists these products with the same active ingredient.

63629-2326 — Haloperidol, 63629-9270 — Haloperidol, 63629-9271 — Haloperidol, 63629-9272 — Haloperidol, 63629-9273 — Haloperidol, 63629-9274 — Haloperidol, 63629-9275 — Haloperidol, 65841-626 — Haloperidol, 65841-627 — Haloperidol, 65841-628 — Haloperidol, 65841-838 — Haloperidol, 65841-839 — Haloperidol, 67046-0053 — Haloperidol, 67046-0329 — Haloperidol, 67046-0838 — Haloperidol, 67046-1255 — Haloperidol, 67046-1496 — haloperidol, 67046-1498 — Haloperidol, 67046-1544 — Haloperidol, 67046-1548 — 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.