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risperidone

NDC 65841-665 · Zydus Lifesciences Limited

Generic namerisperidone
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)RISPERIDONE
Strength.25 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

65841-665-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65841-665-01)

65841-665-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65841-665-05)

65841-665-06 — 30 TABLET, FILM COATED in 1 BOTTLE (65841-665-06)

65841-665-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (65841-665-10)

65841-665-14 — 60 TABLET, FILM COATED in 1 BOTTLE (65841-665-14)

65841-665-16 — 90 TABLET, FILM COATED in 1 BOTTLE (65841-665-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-264 — RISPERIDONE, 63187-418 — risperidone, 63187-439 — RISPERIDONE, 63187-642 — RISPERIDONE, 63304-643 — Risperidone, 63304-644 — Risperidone, 63304-949 — Risperidone, 63304-950 — Risperidone, 63304-951 — Risperidone, 65162-673 — Risperidone, 65841-666 — risperidone, 65841-667 — risperidone, 65841-668 — risperidone, 65841-669 — risperidone, 65841-670 — risperidone, 65862-167 — RISPERIDONE, 67046-0630 — RISPERIDONE, 67046-0635 — RISPERIDONE, 67046-0644 — RISPERIDONE, 67046-2064 — 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.