Risperidone

NDC 69238-2108 · Amneal Pharmaceuticals NY LLC

Generic nameRisperidone

Dosage formTABLET

RouteORAL

Active ingredient(s)RISPERIDONE

Strength.25 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

69238-2108-5 — 500 TABLET in 1 BOTTLE (69238-2108-5)

69238-2108-6 — 60 TABLET in 1 BOTTLE (69238-2108-6)

FDA lists these products with the same active ingredient.

68084-272 — Risperidone, 68084-273 — Risperidone, 68084-274 — Risperidone, 68084-277 — Risperidone, 68382-112 — risperidone, 68382-113 — risperidone, 68382-114 — risperidone, 68382-115 — risperidone, 68382-116 — risperidone, 68382-117 — risperidone, 69238-2109 — Risperidone, 69238-2110 — Risperidone, 69238-2111 — Risperidone, 69238-2112 — Risperidone, 69238-2113 — Risperidone, 69292-571 — Risperidone, 69292-572 — Risperidone, 69292-573 — Risperidone, 69292-574 — Risperidone, 69292-575 — 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.