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
- 65841-670_d39bd21c-64bb-4eff-8713-5a5ed9b98c9d
- Product NDC
- 65841-670
- Form
- TABLET, FILM COATED
- Composition / generic term
- risperidone
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081113
- Source listing expiry
- 20261231
Source-listed ingredients
- RISPERIDONE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65841-670-01) · 65841-670-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65841-670-05) · 65841-670-05
- 30 TABLET, FILM COATED in 1 BOTTLE (65841-670-06) · 65841-670-06
- 1000 TABLET, FILM COATED in 1 BOTTLE (65841-670-10) · 65841-670-10
- 60 TABLET, FILM COATED in 1 BOTTLE (65841-670-14) · 65841-670-14
- 90 TABLET, FILM COATED in 1 BOTTLE (65841-670-16) · 65841-670-16
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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