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
- 71205-520_be1f8d5f-876a-4c16-b504-8812d781e06d
- Product NDC
- 71205-520
- Form
- TABLET
- Composition / generic term
- RISPERIDONE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140328
- Source listing expiry
- 20261231
Source-listed ingredients
- RISPERIDONE — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71205-520-30) · 71205-520-30
- 60 TABLET in 1 BOTTLE (71205-520-60) · 71205-520-60
- 90 TABLET in 1 BOTTLE (71205-520-90) · 71205-520-90
Source and coverage
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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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