AMINOSYN 3.5% M
LOE Approachingamino acids; magnesium acetate; phosphoric acid; potassium acetate; sodium chloride
NDAINJECTIONINJECTABLE
Approved
May 1976
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
1/8 — Limited
Drug data last refreshed 1w ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
AMINOSYN 3.5% M is an injectable amino acid formulation with electrolytes (magnesium acetate, potassium acetate, sodium chloride) and phosphoric acid used for parenteral nutrition support. It provides essential amino acids and minerals to patients unable to meet nutritional requirements via oral intake, supporting protein synthesis and metabolic homeostasis. This is a foundational nutritional product administered intravenously in hospital and clinical settings.
LOE Approaching
Product approaching loss of exclusivity with moderate competitive pressure (30), indicating defensive positioning and focus on manufacturing excellence and cost control rather than growth 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
Working on AMINOSYN 3.5% M offers career opportunities primarily in operations-focused roles—manufacturing, quality assurance, supply chain, and engineering—reflecting the product's mature lifecycle and commodity-like competitive dynamics. This is an ideal environment for professionals seeking to develop expertise in pharmaceutical manufacturing, regulatory compliance, and cost optimization in a stable, non-launch environment.
Engineer
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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.