risperidone · Janssen Pharms · NDA 020272, 020588, 021444

Risperdal

Earliest generic entry, as listed · earliest of 7 marketed strengths
Open now

No unexpired patents or exclusivities are listed for this product.

Listed patents · 0 unexpired

No unexpired patents listed.

Exclusivities · 0 unexpired

No unexpired exclusivities listed.

Paragraph IV certifications · 0

No Paragraph IV certification listed by FDA for this drug.

The list shows that a generic applicant certified to FDA that a listed patent is invalid or not infringed. It does not show litigation, settlements or launch timing.

Event history

No events yet. The first ingestion only records products entering their 12-month window; changes appear from the next Orange Book update.

Products covered · 13

NDA · productFormStrengthListed expiry
020272 · 001 · RLDtablet, oral1MGopen
020272 · 002 · RLDtablet, oral2MGopen
020272 · 003 · RLDtablet, oral3MGopen
020272 · 004 · RLDtablet, oral4MGopen
020272 · 005 · discontinuedtablet, oral5MGopen
020272 · 007 · RLDtablet, oral0.5MGopen
020272 · 008 · RLDtablet, oral0.25MGopen
020588 · 001 · RLDsolution, oral1MG/MLopen
021444 · 001 · RLD · discontinuedtablet, orally disintegrating, oral0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
021444 · 002 · RLD · discontinuedtablet, orally disintegrating, oral1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
021444 · 003 · RLD · discontinuedtablet, orally disintegrating, oral2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
021444 · 004 · RLD · discontinuedtablet, orally disintegrating, oral3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
021444 · 005 · RLD · discontinuedtablet, orally disintegrating, oral4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open