molindone hydrochloride · Chartwell Rx · NDA 017111, 017938

Moban

Earliest generic entry, as listed · earliest of 8 marketed strengths
Open now

No marketed reference-listed strength; date taken from all listed strengths.

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 · 9

NDA · productFormStrengthListed expiry
017111 · 001 · RLD · discontinuedcapsule, oral5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 002 · RLD · discontinuedcapsule, oral10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 003 · RLD · discontinuedcapsule, oral25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 004 · RLD · discontinuedtablet, oral5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 005 · RLD · discontinuedtablet, oral10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 006 · RLD · discontinuedtablet, oral25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 007 · RLD · discontinuedtablet, oral50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017111 · 008 · RLD · discontinuedtablet, oral100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017938 · 001 · discontinuedconcentrate, oral20MG/MLopen