United States · FDA National Drug Code directory

Risperidone

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
59746-225_39d41b28-93eb-446b-9652-7432858ccbab
Product NDC
59746-225
Form
TABLET
Composition / generic term
Risperidone
Labeler
Jubilant Cadista Pharmacuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20251015
Source listing expiry
20261231

Source-listed ingredients

  • RISPERIDONE — 3 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 TABLET in 1 BOTTLE (59746-225-05) · 59746-225-05
  • 60 TABLET in 1 BOTTLE (59746-225-60) · 59746-225-60

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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