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Risperidone

NDC 69367-369 · Westminster Pharmaceuticals, LLC

Generic nameRisperidone
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)RISPERIDONE
Strength.5 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

69367-369-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-369-05)

69367-369-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-369-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69292-573 — 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, 69367-370 — Risperidone, 69367-371 — Risperidone, 69367-372 — Risperidone, 69367-373 — Risperidone, 70518-0364 — RISPERIDONE, 70518-1502 — RISPERIDONE, 70518-1568 — RISPERIDONE, 70518-1575 — RISPERIDONE, 70518-1613 — RISPERIDONE, 70518-1771 — 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.