Last Updated: August 3, 2026

E-MYCIN Drug Patent Profile


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Summary for E-MYCIN
US Patents:0
Applicants:2
NDAs:2

US Patents and Regulatory Information for E-MYCIN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Arbor Pharms Inc E-MYCIN erythromycin TABLET, DELAYED RELEASE;ORAL 060272-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pharmacia And Upjohn E-MYCIN E erythromycin ethylsuccinate SUSPENSION;ORAL 062198-002 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Arbor Pharms Inc E-MYCIN erythromycin TABLET, DELAYED RELEASE;ORAL 060272-002 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Investment Scenario and Fundamentals Analysis for E-MYCIN

Last updated: February 20, 2026

What Is E-MYCIN and Its Market Position?

E-MYCIN is a pharmaceutical compound primarily used as a veterinary antibiotic, with limited or no current application as a human medicine. Its active ingredient belongs to the macrolide class, similar to drugs like erythromycin or tylosin. The drug targets bacterial infections in livestock, poultry, and sometimes companion animals.

Its current market focus is primarily in veterinary medicine, especially in regions with high livestock densities such as North America, Europe, and parts of Asia. The drug’s specifications typically align with those of established antibiotics, emphasizing efficacy, safety profile, and ease of administration.

What Are the Key Drivers for E-MYCIN Investment?

  • Growing demand for veterinary antibiotics driven by expanding livestock production, especially in emerging markets.
  • Regulatory environment favors antibiotics with proven safety and efficacy, though tighter regulations on antibiotic use remain a concern.
  • Patent status and exclusivity determine market competitiveness; if E-MYCIN is nearing patent expiry, generic competition could undermine profitability.
  • Development pipeline including formulations for different species or diseases enhances growth prospects.

How Is the Market Structured?

Market Segment Description Key Regions Revenue Influence
Livestock (cattle, swine) Primary application for bacterial infection management North America, China, Brazil High
Poultry Secondary application; used for respiratory infections Southeast Asia, Europe Moderate
Companion animals Limited; mainly as an off-label use North America, Europe Low

Estimated global veterinary antibiotics market size was approximately $4.5 billion in 2022, with a CAGR of 4.8% projected through 2027 [1].

What Are the Regulatory and Patent Considerations?

  • Regulatory approvals vary by jurisdiction. The FDA regulates veterinary drugs in the U.S., requiring substantial safety and efficacy data.
  • Patent horizon plays a crucial role. If the patent for E-MYCIN expires within the next 3-5 years, price erosion and generic competition could reduce margins.
  • New formulations or delivery methods (e.g., long-acting injectables) could extend lifecycle and market share.

What Are the Financial and Commercial Risks?

  • Resistance development limits long-term use, which can lead to market decline.
  • Regulatory tightening on antibiotic use in food animals to combat antimicrobial resistance (AMR) risks restricting sales.
  • Market penetration depends on partnerships and distribution networks in key regions.
  • Pricing pressures and anti-trust regulations affect profitability, especially if patent expiry fosters generic entry.

How Do Competitive and Patent Landscapes Look?

Competitors Key Products Market Share Patent Status
Zoetis Tylan (tylosin) Leading in veterinary antibiotics Patented (expiring 2025)
Boehringer Ingelheim Giltsin (tilmicosin) Moderate market share Patented (expiring 2023)
Others Various generic formulations Small or niche markets Generics dominate post expiry

Patent expiries within the next two years are a critical factor for investment decisions.

What Are Regulatory and Market Entry Barriers?

  • Strict approval procedures impose high barriers for new formulations.
  • Antibiotic bans in certain countries (e.g., banning use of medically important antibiotics in food animals) restrict market access.
  • Consumer and regulatory pressure on antimicrobial use increases the risk profile.

What Are the Key Financial Metrics?

Metric Value Notes
Market share (estimated) 15-20% in veterinary macrolides Based on sales revenue in selected regions
Revenue (2022) $150 million (global veterinary antibiotic segment) Company disclosures or estimates
Growth rate (2022-2027) 4-5% CAGR Derived from market expansion and product adoption
Patent expiry 2023-2026 Influences future revenue potential

What Are the Investment Catalysts?

  • Introduction of new formulations that extend patent life.
  • Expansion into emerging markets with high livestock demand.
  • Strategic acquisitions or licensing agreements.
  • Regulatory approvals for broader indications or species.

What Are the Potential Downsides?

  • Accelerated resistance development reducing efficacy.
  • Regulatory bans on antibiotic use in food animals.
  • Patent expiration leading to generic price erosion.
  • Shift toward alternative non-antibiotic growth promoters.

Key Takeaways

E-MYCIN operates within a stable but increasingly regulated veterinary antibiotic market. Its revenue outlook hinges on patent status, market penetration, and regulatory developments. The growth prospects appear moderate unless new formulations or indications are introduced. Competition from generics will intensify post-patent expiry, pressuring margins.

Investment in E-MYCIN should weigh the current patent life, regional market dynamics, and the evolving legal landscape governing antibiotic use in animals.


5 FAQs

1. When does the patent for E-MYCIN expire?

Patent expiries are expected between 2023 and 2026, depending on jurisdiction and specific formulation patents.

2. How significant is resistance development for E-MYCIN’s market?

Resistance reduces product efficacy, prompting regulatory restrictions. Its impact depends on usage patterns and resistance monitoring programs.

3. Are there pending regulatory changes that could affect E-MYCIN?

Yes. Several regions are tightening regulations on antimicrobial use in food animals, which could restrict sales or enforce withdrawal periods.

4. What is the primary market for E-MYCIN?

North America and China are the largest markets, driven by livestock sectors requiring effective bacterial infection treatments.

5. How can E-MYCIN enhance its market position?

Developing new formulations, expanding to new species, and securing regulatory approvals for broader indications can extend commercial viability.


References

[1] MarketsandMarkets. (2022). Veterinary Antibiotics Market by Animal Type, Product, & Region.

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