Risperidone

NDC 63304-643 · Sun Pharmaceutical Industries, Inc.

Generic nameRisperidone

Dosage formTABLET, ORALLY DISINTEGRATING

RouteORAL

Active ingredient(s)RISPERIDONE

Strength3 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

63304-643-05 — 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-643-05)

63304-643-17 — 10 POUCH in 1 BOX, UNIT-DOSE (63304-643-17) / 1 TABLET, ORALLY DISINTEGRATING in 1 POUCH (63304-643-11)

63304-643-30 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-643-30)

63304-643-69 — 1 BLISTER PACK in 1 CARTON (63304-643-69) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

62135-602 — Risperidone, 62135-603 — Risperidone, 62135-604 — Risperidone, 62135-605 — Risperidone, 62135-929 — RISPERIDONE, 62559-981 — Risperidone, 63187-264 — RISPERIDONE, 63187-418 — risperidone, 63187-439 — RISPERIDONE, 63187-642 — 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, 65841-669 — 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.