Haloperidol

NDC 0121-0581 · PAI Holdings, LLC dba PAI Pharma

Generic nameHaloperidol

Dosage formSOLUTION

RouteORAL

Active ingredient(s)HALOPERIDOL

Strength2 mg/mL

Pharmacologic classTypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

0121-0581-04 — 120 mL in 1 BOTTLE (0121-0581-04)

0121-0581-05 — 10 TRAY in 1 CASE (0121-0581-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE

0121-0581-15 — 15 mL in 1 BOTTLE (0121-0581-15)

FDA lists these products with the same active ingredient.

0378-0214 — haloperidol, 0378-0257 — haloperidol, 0378-0327 — haloperidol, 0378-0351 — haloperidol, 0615-8626 — haloperidol, 0615-8627 — haloperidol, 0832-1510 — Haloperidol, 0832-1520 — Haloperidol, 0832-1530 — Haloperidol, 0832-1540 — Haloperidol, 0832-1550 — Haloperidol, 0832-1560 — Haloperidol, 0904-6661 — Haloperidol, 0904-6733 — Haloperidol, 0904-6782 — Haloperidol, 0904-7504 — haloperidol, 10135-752 — Haloperidol, 10135-753 — Haloperidol, 10135-754 — Haloperidol, 10135-755 — 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.