United States · FDA National Drug Code directory
Latuda
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
- 63402-302_7383b0e0-01e8-4778-96f0-6f2e0c9586ae
- Product NDC
- 63402-302
- Form
- TABLET, FILM COATED
- Composition / generic term
- lurasidone hydrochloride
- Labeler
- Sumitomo Pharma America, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20111207
- Source listing expiry
- 20271231
Source-listed ingredients
- LURASIDONE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 BLISTER PACK in 1 CARTON (63402-302-04) / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-07) · 63402-302-04
- 10 BLISTER PACK in 1 CARTON (63402-302-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-302-01) · 63402-302-10
- 30 TABLET, FILM COATED in 1 BOTTLE (63402-302-30) · 63402-302-30
- 500 TABLET, FILM COATED in 1 BOTTLE (63402-302-50) · 63402-302-50
- 90 TABLET, FILM COATED in 1 BOTTLE (63402-302-90) · 63402-302-90
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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