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Data updated: Jun 28, 2026

TARO

Generics

TARO is a generic drug manufacturer focused on Neurology, Dermatology, Cardiovascular.

1977
Since
85
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
3 Small Molecules

TARO's Key Drugs

TARO's core commercial portfolio centers on BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE, SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE, spanning Neurology and Dermatology — its most strategically important drugs approved in the last 15 years.

TARO's Recent FDA Approvals

New NDA/BLA approvals for TARO over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

TARO's Therapeutic Areas

TARO's approved drugs and pipeline span 5 therapeutic areas, led by Neurology and Dermatology, across 0 biologic and 3 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Neurology 39%
9 drugs
Dermatology 17%
4 drugs
Cardiovascular 17%
4 drugs
Oncology 13%
3 drugs
Gastroenterology 13%
3 drugs

TARO's Top Competitors

TARO's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Baxter, and Eli Lilly. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

TARO Pipeline Snapshot

Active clinical trials for TARO across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE leads revenue
  • 2 key drugs tracked

Trial Catalysts

  • Neurology pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

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  • Side-by-side pipeline analysis
  • Revenue & market share comparison
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