doxepin hydrochloride · Pfizer · NDA 016798, 017516

Sinequan

Earliest generic entry, as listed · earliest of 7 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 · 7

NDA · productFormStrengthListed expiry
016798 · 001 · RLD · discontinuedcapsule, oralEQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
016798 · 002 · RLD · discontinuedcapsule, oralEQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
016798 · 003 · RLD · discontinuedcapsule, oralEQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
016798 · 005 · RLD · discontinuedcapsule, oralEQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
016798 · 006 · RLD · discontinuedcapsule, oralEQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
016798 · 007 · RLD · discontinuedcapsule, oralEQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open
017516 · 001 · RLD · discontinuedconcentrate, oralEQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**open