SOLODYN
PeakNDAORALTABLET, EXTENDED RELEASE
Approved
May 2006
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
1
Data completeness
4/8 — Partial
Drug data last refreshed 14h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
SOLODYN is an extended-release oral minocycline tablet approved for treating inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years and older. The mechanism of action for acne treatment remains unknown, though minocycline is lipid-soluble and distributes into skin and sebum. SOLODYN provides delayed absorption compared to immediate-release minocycline formulations.
$0.004BPart D
Peak5.0 years to LOEProduct is at peak lifecycle with modest Part D utilization; brand team focus likely on maintenance and defending against generic competition.
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.
Clinical Trials (1)
A Comparative Bioavailability Study of DFD-29 Capsules 40 mg Versus SOLODYN® Tablets 105 mg, Under Fasting & Fed Conditions in Healthy Adult Human Subjects
Started May 2022
24 enrolled
Pharmacokinetics
Career Relevance
SOLODYN positions you in a stable, mature brand with modest commercial footprint and zero linked job openings currently visible. This role offers experience in lifecycle management and defensive strategy rather than growth acceleration or innovation, ideal for professionals seeking stability in a commodity market segment.
Brand Manager
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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.