Risperidone

NDC 69367-373 · Westminster Pharmaceuticals, LLC

Generic nameRisperidone

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RISPERIDONE

Strength4 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

69367-373-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-373-05)

69367-373-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-373-60)

FDA lists these products with the same active ingredient.

69339-182 — Risperidone, 69339-183 — Risperidone, 69339-184 — Risperidone, 69339-185 — Risperidone, 69339-186 — Risperidone, 69367-368 — Risperidone, 69367-369 — Risperidone, 69367-370 — Risperidone, 69367-371 — Risperidone, 69367-372 — Risperidone, 70518-0364 — RISPERIDONE, 70518-1502 — RISPERIDONE, 70518-1568 — RISPERIDONE, 70518-1575 — RISPERIDONE, 70518-1613 — RISPERIDONE, 70518-1771 — RISPERIDONE, 70518-3741 — Risperidone, 70518-3760 — risperidone, 70518-3883 — Risperidone, 70518-4426 — Risperidone, +159 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.