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Risperidone

NDC 69339-182 · Natco Pharma USA LLC

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

Packages

69339-182-03 — 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69339-182-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 69339-181 — Risperidone, 69339-183 — Risperidone, 69339-184 — Risperidone, 69339-185 — Risperidone, 69339-186 — Risperidone, 69367-368 — Risperidone, 69367-369 — Risperidone, 69367-370 — Risperidone, 69367-371 — Risperidone, 69367-372 — Risperidone, 69367-373 — 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.