WATSON LABS INC
GenericsWATSON LABS INC is a generic drug manufacturer focused on Cardiovascular, Neurology, Infectious Disease.
WATSON LABS INC at a Glance
- Strong track record with 83% execution quality across 12 trials
- Fast trial execution (9 months median completion)
WATSON LABS INC's Key Drugs
WATSON LABS INC's core commercial portfolio centers on DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM, NORGESTIMATE; ETHINYL ESTRADIOL, spanning Cardiovascular and Neurology — its most strategically important drugs approved in the last 15 years.
WATSON LABS INC's Recent FDA Approvals
WATSON LABS INC secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.
WATSON LABS INC's Therapeutic Areas
WATSON LABS INC's approved drugs and pipeline span 5 therapeutic areas, led by Cardiovascular and Neurology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.
WATSON LABS INC's Top Competitors
WATSON LABS INC's closest competitors by therapeutic-area and drug-target overlap include Pfizer, PAI HOLDINGS PHARM, and BAUSCH AND LOMB INC. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.
WATSON LABS INC Pipeline Snapshot
Active clinical trials for WATSON LABS INC across all therapeutic areas, from ClinicalTrials.gov.
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Deep insights for investors and analysts
Revenue Insights
- • DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM leads revenue
- • 2 key drugs tracked
Trial Catalysts
- • Cardiovascular 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: 1/2 completed
- • Speed: 9 months avg
Revenue forecasts • Trial milestones • Patent risk modeling
Discontinued (2)
Company Info
- First Approval
- 1971-12-22
- Latest
- 2026-06-18
- Applications
- 987
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 Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.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