DURAGESIC-12
LOE ApproachingNDATRANSDERMALFILM, EXTENDED RELEASE
Approved
Aug 1990
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
1/8 — Limited
Drug data last refreshed Yesterday · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
DURAGESIC-12 is a transdermal extended-release film formulation approved in 1990 by Johnson & Johnson. The specific indication and mechanism of action are not disclosed in available data. This product represents a mature, established therapy in its pharmacological class.
LOE Approaching
Product is in late-stage lifecycle with moderate competitive pressure (30), suggesting defensive team positioning and likely focus on retention and cost management initiatives.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
DURAGESIC-12 currently shows zero linked job openings, reflecting its mature LOE-approaching lifecycle stage. Career opportunities on this product emphasize defensive commercial strategy, regulatory compliance, and transition planning rather than growth or innovation roles.
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.