Haloperidol

NDC 68382-081 · Zydus Pharmaceuticals USA Inc.

Generic nameHaloperidol

Dosage formTABLET

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength20 mg/1

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

68382-081-01 — 100 TABLET in 1 BOTTLE (68382-081-01)

68382-081-06 — 30 TABLET in 1 BOTTLE (68382-081-06)

FDA lists these products with the same active ingredient.

67046-1496 — haloperidol, 67046-1498 — Haloperidol, 67046-1544 — Haloperidol, 67046-1548 — Haloperidol, 67046-1603 — Haloperidol, 67046-1673 — Haloperidol, 68084-249 — Haloperidol, 68084-250 — Haloperidol, 68382-079 — Haloperidol, 68382-080 — Haloperidol, 68382-407 — Haloperidol, 68382-408 — Haloperidol, 68382-409 — Haloperidol, 69292-580 — Haloperidol, 69292-582 — Haloperidol, 69292-584 — Haloperidol, 69292-586 — Haloperidol, 69292-588 — Haloperidol, 69292-590 — Haloperidol, 70518-1182 — 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.