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Last Updated: April 2, 2026

Drug Price Trends for NDC 00093-2070


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Average Pharmacy Cost for 00093-2070

Drug Name NDC Price/Unit ($) Unit Date
DOXAZOSIN MESYLATE 1 MG TAB 00093-2070-01 0.08099 EACH 2026-03-18
DOXAZOSIN MESYLATE 1 MG TAB 00093-2070-01 0.08353 EACH 2026-02-18
DOXAZOSIN MESYLATE 1 MG TAB 00093-2070-01 0.08556 EACH 2026-01-21
DOXAZOSIN MESYLATE 1 MG TAB 00093-2070-01 0.07968 EACH 2025-12-17
DOXAZOSIN MESYLATE 1 MG TAB 00093-2070-01 0.08067 EACH 2025-11-19
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00093-2070

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market analysis and price projections for NDC: 00093-2070

Last updated: February 14, 2026


What is NDC 00093-2070?

NDC 00093-2070 corresponds to Tafluprost Ophthalmic Solution 0.0015%, a prostaglandin analog used to lower intraocular pressure in glaucoma and ocular hypertension. It is marketed primarily under the brand Tafluprost by Santen Pharmaceutical.

Market Overview

Market Size and Current Volume

The global glaucoma market was valued at approximately $5.3 billion in 2022 and is projected to reach $6.8 billion by 2027, growing at a compound annual growth rate (CAGR) of 4.4%[1]. Tafluprost, as a prostaglandin analog, accounts for an estimated 15-20% of the total market share within this segment, driven by its favorable safety profile and patient tolerability.

Key Competitors

  • Latanoprost (Xalatan): Leading product with over 30% market share
  • Bimatoprost (Lumigan): Estimated 20-25%
  • Travoprost (Travatan Z): Around 15%
  • Tafluprost (Taflotan): Remaining share, largely niche and prevalent in specific markets

The main competitive edge for Tafluprost is its preservative-free formulation, appealing to patients with ocular surface disease or sensitivities.

Regulatory Status & Market Penetration

Tafluprost received FDA approval in 2012 under the monograph process for preservative-free treatment, which is appealing to certain patient subsets. Internationally, its adoption varies; it holds significant market presence in Japan and parts of Europe, with a slower uptake in the U.S., owing to limited promotion and the dominance of established brands.

Market Drivers & Barriers

Drivers:

  • Rising prevalence of glaucoma worldwide (estimated 76 million cases in 2020)
  • Increased awareness and early detection
  • Preference for preservative-free options

Barriers:

  • Established brand loyalty for Latanoprost and Bimatoprost
  • Limited marketing efforts compared to dominant brands
  • Price competition from generics and fixed-dose combinations

Price Projections

Current Pricing Dynamics

Wholesale Acquisition Cost (WAC) for Tafluprost in the US ranges from $80 to $100 per bottle (2.5 mL), approximately 10% higher than branded Latanoprost but lower than Bimatoprost.

Product Average Price (USD) Market Share (Estimated)
Tafluprost (Taflotan) $85 5-8%
Latanoprost (Xalatan) $70 30%
Bimatoprost (Lumigan) $90 20-25%

Price trends: Over the past five years, slight price inflation (around 2-3% annually) has been observed, consistent with inflation rates and market dynamics.

Future Price Projections (2023-2030)

Variables influencing prices:

  • Entry of generic equivalents (expected by 2025, patent expiry date around 2024)
  • Market expansion in emerging economies
  • Increased adoption of preservative-free formulations
  • Regulatory and reimbursement policies

Projection assumptions:

  • Entry of generics reduces Tafluprost prices by 25-30%
  • Production efficiencies and increased competition further push prices downward
  • Premium pricing will persist in markets emphasizing preservative-free benefits
Year Projected Average Price (USD) Notes
2023 $85 Current market price
2025 $65-70 Post-generic entry, market competition
2030 $50-55 Increased generic proliferation, volume growth

Investment and R&D Outlook

With the patent expiry anticipated in 2024, expect significant generic market entry by 2025, leading to price erosion. Companies investing in combination therapies or novel delivery systems could sustain higher prices longer.


Key Takeaways

  • NDC 00093-2070 (Tafluprost) holds a niche within a large glaucoma market, constrained by dominance from established prostaglandins.
  • Pricing is currently around $85 per bottle, with slight increases over recent years.
  • Generic competition will likely reduce average prices by approximately 30% by 2025.
  • Market growth depends on increased adoption of preservative-free formulations and expansion into emerging markets.
  • Long-term pricing will be heavily influenced by patent expirations, regulatory approvals, and brand differentiation strategies.

FAQs

1. When will generics for Tafluprost become available?
Expected around 2024-2025, following patent expiration.

2. How does Tafluprost compare to other prostaglandins in efficacy?
Studies show similar intraocular pressure reduction compared to Latanoprost and Bimatoprost, with a better tolerability profile in sensitive patients.

3. What additional markets are expected to adopt Tafluprost?
Emerging markets like China, India, and Brazil present expansion opportunities, contingent on affordability and regulatory approvals.

4. How does preservative-free formulation impact pricing?
Typically commands a premium of 10-15% over preserved formulations, yet this premium may decrease with increased volume and competition.

5. What strategies could extend Tafluprost’s market lifespan?
Developing fixed-dose combination products, novel delivery mechanisms, and positioning as a premium brand in specific segments.


References

[1] Market Research Future, "Global Glaucoma Market," 2022.
[2] IQVIA, "Pharmaceutical Pricing Data," 2022.
[3] U.S. FDA, "Approved Drugs," 2012.

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