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Last Updated: December 11, 2025

Teligent Company Profile


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What is the competitive landscape for TELIGENT

TELIGENT has five approved drugs.



Summary for Teligent
US Patents:0
Tradenames:5
Ingredients:5
NDAs:5

Drugs and US Patents for Teligent

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Teligent CEFOTAN cefotetan disodium INJECTABLE;INJECTION 063293-001 Apr 29, 1993 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teligent M.V.I.-12 LYOPHILIZED ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine; riboflavin 5'-phosphate sodium; thiamine; vitamin a; vitamin e INJECTABLE;INJECTION 018933-002 Aug 8, 1985 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teligent DOBUTAMINE HYDROCHLORIDE dobutamine hydrochloride INJECTABLE;INJECTION 074098-001 Feb 21, 1995 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teligent FLURANDRENOLIDE flurandrenolide OINTMENT;TOPICAL 207851-001 Dec 30, 2016 RX No Yes ⤷  Get Started Free ⤷  Get Started Free
Teligent CEFOTAN cefotetan disodium INJECTABLE;INJECTION 063293-002 Apr 29, 1993 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teligent DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 018656-001 Jun 28, 1983 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration
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Pharmaceutical Competitive Landscape Analysis: Teligent – Market Position, Strengths & Strategic Insights

Last updated: July 27, 2025


Introduction

Teligent Inc. stands as a notable entity within the pharmaceutical industry, primarily focusing on the development, manufacturing, and commercialization of generic and specialty pharmaceuticals. Operating in a highly competitive landscape marked by patent expirations, aggressive market entrants, and evolving regulatory frameworks, Teligent’s strategic positioning warrants detailed analysis. This report dissects Teligent's current market posture, core strengths, competitive advantages, and strategic pathways to sustain growth amid industry volatility.


Market Position Overview

Company Profile and Financial Metrics

Founded in 1993 and based in Buena, New Jersey, Teligent has carved a niche in sterile and topical generics products. As of 2022, the firm’s revenue streams predominantly stem from sterile injectables and topical formulations, accounting for approximately 70% of its sales [1]. Despite a fragmented and competitive market, Teligent has maintained a modest but steady market share, estimated at around 2-3% of the U.S. generic pharmaceutical market—a sector valued at over $140 billion [2].

Competitive Landscape Context

Teligent operates amidst a dense field of generic players, including Teva, Mylan (now part of Viatris), Sandoz, and inductively, emerging specialty firms. The industry exhibits high patent expiration rates, creating an influx of opportunities but also intensifies price competition. Teligent’s niche focus on sterile injectables positions it uniquely, as demand for these formulations continues to grow, driven by hospital and oncology-market needs.

Market Challenges and Opportunities

The firm faces considerable challenges, including regulatory hurdles, manufacturing capacity constraints, and aggressive pricing pressures. Conversely, opportunities arise from the increasing demand for specialized injectables, regulatory incentives for orphan drugs, and the expanding pipeline of biosimilars and complex generics.


Strengths of Teligent

Specialized Manufacturing Capabilities

Teligent’s dedicated focus on sterile and topical formulations boosts its competitive advantage through high-quality manufacturing standards. This specialization minimizes reliance on third-party manufacturing, reducing supply chain vulnerabilities, and fostering regulatory compliance. Its FDA-approved manufacturing facility in Buena, NJ, is FDA and DEA compliant, supporting complex sterile injectable production.

Robust Product Portfolio

The company manifests a portfolio with over 50 marketed products, including critical sterile injectables used across oncology, vaccines, and infectious disease sectors. This diversified product range mitigates risks associated with dependency on a limited set of high-revenue products and offers cross-selling opportunities [3].

Regulatory Expertise and Quality Standards

Teligent’s proactive compliance with regulatory standards and transparent quality practices facilitate smoother product approvals and renewals. Its recent re-inspection cycles by the FDA reaffirm adherence to Good Manufacturing Practices (GMP), enabling it to maintain product integrity and market access.

Strategic Collaborations and Licensing

Partnerships with outsourcing and distribution entities expand Teligent’s market reach, particularly in hospital and clinic settings. Licensing agreements facilitate product diversification with minimal capital expenditure, ensuring a faster time to market.


Strategic Insights

Focus on High-Margin, Complex Generics

Given the commoditization of many basic generics, Teligent’s emphasis on complex generics and biosimilars can unlock higher margins and reduce price competition. The rising prevalence of biosimilars, projected to grow at a CAGR of 27% through 2027 [4], represents a key axis for expansion.

Investments in R&D and Pipeline Development

Innovative pipeline expansion is critical. Focused R&D on complex injectables, drug-device combination products, and niche therapeutic areas like ophthalmics or dermatologics could establish market differentiation. Strategic alliances with biotech firms for biosimilars development also offer substantial upside.

Operational Optimization and Capacity Enhancement

Scaling manufacturing capacity through capacity investments or facility upgrades could mitigate current supply constraints. Modernizing production lines for high-efficiency sterile processes and expanding capacity in response to rising demand will be pivotal.

Regulatory and Market Expansion Strategies

Proactive engagement with global regulatory agencies enables faster approvals in European, Asian, and emerging markets. Expanding into these regions diversifies revenue streams and alleviates pressure from U.S. market dynamics.

Acquisition and Partnership Strategies

Selective acquisitions of niche analgesic, oncologic, or dermatologic assets can accelerate growth and diversify the portfolio. Forming strategic alliances with specialty distributors can further penetrate hospital systems and outpatient clinics.


Competitive Advantages and Risks

Advantages

  • Niche Focus: Specialization in sterile injectables offers a barrier to entry against broad-spectrum generic manufacturers.
  • Regulatory Compliance: Proven adherence to standards enhances trust and reduces time-to-market for new products.
  • Product Diversification: Wide portfolio reduces revenue dependence on individual products, shielding against market disruptions.
  • Partnership Network: Effective licensing and distribution networks extend market coverage.

Risks

  • Manufacturing Disruptions: Supply chain interruptions or quality issues could hamper product availability.
  • Pricing Pressures: Ongoing cost-based competition often erodes margins.
  • Regulatory Hurdles: Increased FDA scrutiny or delays can impact product launches.
  • Market Saturation: Intense competition in key segments could limit growth potential.

Conclusion

Teligent's strategic positioning hinges on its specialized manufacturing capabilities, diversified portfolio, and regulatory expertise. To enhance its competitive stance, the company must prioritize pipeline innovation in complex generics and biosimilars, expand manufacturing capacity, and explore new geographic markets. Maintaining agility in regulatory compliance and forging strategic alliances will further solidify its market share, particularly amidst an evolving pharmaceutical landscape characterized by persistent pressures and unprecedented opportunities.


Key Takeaways

  • Leverage Niche Market Specialization: Teligent’s focus on sterile injectables positions it favorably for growth driven by increasing hospital and outpatient demand.
  • Invest in R&D and Product Pipeline: Expanding complex generics and biosimilars pipeline is essential to offset commoditization and enhance margins.
  • Enhance Manufacturing Capabilities: Capacity upgrades and technological modernization will improve operational resilience and market responsiveness.
  • Strategic Geographic Expansion: Penetrating international markets through regulatory and distribution partnerships diversifies revenue streams.
  • Form Strategic Alliances: Licensing and acquisition strategies can accelerate growth and diversify product offerings, mitigating risks of market saturation.

FAQs

Q1: How does Teligent differentiate itself from other generic pharmaceutical companies?
A1: Teligent’s differentiation stems from its specialized focus on sterile injectables and topical formulations, high-quality manufacturing standards, and regulatory expertise, enabling it to serve niche markets less accessible to broader generic competitors.

Q2: What are the main growth drivers for Teligent in the foreseeable future?
A2: Growth drivers include expanding its complex generics and biosimilars pipeline, increasing manufacturing capacity, entering international markets, and securing strategic partnerships with biotech and distribution firms.

Q3: What risks could hinder Teligent’s strategic growth?
A3: Risks include manufacturing disruptions, intense price competition, regulatory delays, and market saturation, especially in commoditized segments of the generic drugs landscape.

Q4: How significant is the biosimilars market for Teligent’s future?
A4: The biosimilars market offers significant growth potential due to favorable regulatory environments and escalating demand; Teligent’s expertise in complex injectables positions it well to capitalize on this trend.

Q5: What strategies should Teligent prioritize for competitive advantage?
A5: Priorities should include pipeline expansion in complex generics and biosimilars, capacity investments, international market entry, and strategic acquisitions or licensing agreements to diversify and strengthen its portfolio.


Sources

  1. Teligent Annual Report 2022
  2. IQVIA Pharmaceutical Market Data 2022
  3. Company website and product portfolio overview
  4. Grand View Research, "Biosimilars Market Analysis," 2022

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