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Data updated: Jun 28, 2026

USL PHARMA

Generics

USL PHARMA is a generic drug manufacturer focused on Neurology, Cardiovascular, Oncology.

1976
Since
56
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
1 Small Molecules

USL PHARMA at a Glance

  • Fast trial execution (22 months median completion)

USL PHARMA's Key Drugs

USL PHARMA's key approved drugs from the last 15 years (excludes generics, biosimilars and IV formulations).

No active drugs

USL PHARMA's Recent FDA Approvals

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

No recent approvals

USL PHARMA's Therapeutic Areas

USL PHARMA's approved drugs and pipeline span 5 therapeutic areas, led by Neurology and Cardiovascular, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Neurology 40%
4 drugs
Cardiovascular 30%
3 drugs
Oncology 10%
1 drugs
Immunology 10%
1 drugs
Gastroenterology 10%
1 drugs

USL PHARMA's Top Competitors

USL PHARMA's closest competitors by therapeutic-area and drug-target overlap include Bristol-Myers Squibb, Pfizer, and Takeda. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

USL PHARMA Pipeline Snapshot

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

No active pipeline data available

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • Top drug revenue breakdown
  • Drug-level revenue analysis

Trial Catalysts

  • Neurology pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

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

Execution Intelligence

  • Phase 3: 2/3 completed
  • Speed: 22 months avg
Unlock Full Intelligence

Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges