TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

DORYX MPC

DOXYCYCLINE HYCLATE
Approved 2005-05-06
5
Indications
--
Phase 3 Trials
1
Priority Reviews
20
Years on Market

Details

Status
Discontinued
First Approved
2005-05-06
Routes
ORAL
Dosage Forms
TABLET, DELAYED RELEASE

Companies

Active Ingredient: DOXYCYCLINE HYCLATE

DORYX MPC Approval History

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What DORYX MPC Treats

5 FDA approvals

Originally approved for its first indication in 2005 . Covers 5 distinct patient populations.

  • Other (5)
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

DORYX MPC FDA Label Details

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DORYX MPC Patents & Exclusivity

Latest Patent: Dec 2034

Patents (28 active)

US9446057 Expires Dec 23, 2034
US9295652 Expires Oct 23, 2034
US9511031 Expires Oct 23, 2034
US8715724 Expires Feb 3, 2028
+ 18 more patents
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.