Risperidone

NDC 49884-212 · Par Health USA, LLC

Generic nameRisperidone

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)RISPERIDONE

Strength.25 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

49884-212-55 — 5 BLISTER PACK in 1 CARTON (49884-212-55) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-212-52)

FDA lists these products with the same active ingredient.

42291-978 — Risperidone, 42291-979 — Risperidone, 43063-254 — Risperidone, 43063-908 — RISPERIDONE, 43547-339 — Risperidone, 43547-340 — Risperidone, 43547-341 — Risperidone, 43547-342 — Risperidone, 43547-343 — Risperidone, 43547-344 — Risperidone, 49884-311 — Risperidone, 49884-315 — Risperidone, 49884-401 — Risperidone, 49884-402 — Risperidone, 49884-403 — Risperidone, 50090-3340 — RISPERIDONE, 50090-3341 — RISPERIDONE, 50458-300 — risperidone, 50458-302 — risperidone, 50458-305 — 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.