risperidone

NDC 65841-669 · Zydus Lifesciences Limited

Generic namerisperidone

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RISPERIDONE

Strength3 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

65841-669-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65841-669-01)

65841-669-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65841-669-05)

65841-669-06 — 30 TABLET, FILM COATED in 1 BOTTLE (65841-669-06)

65841-669-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (65841-669-10)

65841-669-14 — 60 TABLET, FILM COATED in 1 BOTTLE (65841-669-14)

65841-669-16 — 90 TABLET, FILM COATED in 1 BOTTLE (65841-669-16)

FDA lists these products with the same active ingredient.

63304-643 — Risperidone, 63304-644 — Risperidone, 63304-949 — Risperidone, 63304-950 — Risperidone, 63304-951 — Risperidone, 65162-673 — Risperidone, 65841-665 — risperidone, 65841-666 — risperidone, 65841-667 — risperidone, 65841-668 — risperidone, 65841-670 — risperidone, 65862-167 — RISPERIDONE, 67046-0630 — RISPERIDONE, 67046-0635 — RISPERIDONE, 67046-0644 — RISPERIDONE, 67046-2064 — Risperidone, 68071-3873 — Risperidone, 68071-4618 — RISPERIDONE, 68084-270 — Risperidone, 68084-271 — 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.