Risperidone

NDC 69292-573 · Amici Pharma, Inc.

Generic nameRisperidone

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)RISPERIDONE

Strength2 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

69292-573-28 — 7 BLISTER PACK in 1 CARTON (69292-573-28) / 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

68382-116 — risperidone, 68382-117 — risperidone, 69238-2108 — Risperidone, 69238-2109 — Risperidone, 69238-2110 — Risperidone, 69238-2111 — Risperidone, 69238-2112 — Risperidone, 69238-2113 — Risperidone, 69292-571 — Risperidone, 69292-572 — Risperidone, 69292-574 — Risperidone, 69292-575 — Risperidone, 69339-181 — Risperidone, 69339-182 — Risperidone, 69339-183 — Risperidone, 69339-184 — Risperidone, 69339-185 — Risperidone, 69339-186 — Risperidone, 69367-368 — Risperidone, 69367-369 — Risperidone, +159 more

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