TheraRadar
Data updated: Jun 28, 2026

CONDYLOX (podofilox) · Teva

Dermatology Approved 1990-12-13

CONDYLOX is FDA-approved to treat 1 condition (same as PODOFILOX).

2
Indications
--
Phase 3 Trials
1
Priority Reviews
35
Years on Market

Details

Status
Discontinued
First Approved
1990-12-13
Routes
TOPICAL
Dosage Forms
SOLUTION, GEL

Companies

Active Ingredient: PODOFILOX

CONDYLOX Approval History

1991
1992
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2026
Original
New Indication
New Form
Label Update
13 FDA actions from 1990 to 2015
Oct 2015 SUPPL Priority
Mfg · Manufacturing (CMC)
Sep 2015 SUPPL Priority
Mfg · Manufacturing (CMC)
Jan 2014 SUPPL Priority
Mfg · Manufacturing (CMC)

What CONDYLOX Treats

1 indications

CONDYLOX is approved for 1 conditions since its original approval in 1990. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Genital Warts

Same approved indications as PODOFILOX (same active ingredient).

Source: FDA Label

Teva's other novel FDA approvals

Other CDER-designated drugs from the same sponsor (2016–2025).

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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.

CONDYLOX FDA Label Details

Indications & Usage

FDA Label (PDF)

CONDYLOX is FDA-approved to treat 1 condition — same approved indications as PODOFILOX.

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Data Sources

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