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Last Updated: April 1, 2026

Drug Price Trends for NDC 57664-0396


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Average Pharmacy Cost for 57664-0396

Drug Name NDC Price/Unit ($) Unit Date
VENLAFAXINE HCL 100 MG TABLET 57664-0396-88 0.12215 EACH 2026-03-18
VENLAFAXINE HCL 100 MG TABLET 57664-0396-88 0.11946 EACH 2026-02-18
VENLAFAXINE HCL 100 MG TABLET 57664-0396-88 0.11439 EACH 2026-01-21
VENLAFAXINE HCL 100 MG TABLET 57664-0396-88 0.10853 EACH 2025-12-17
VENLAFAXINE HCL 100 MG TABLET 57664-0396-88 0.10513 EACH 2025-11-19
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 57664-0396

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
VENLAFAXINE HCL 100MG TAB Golden State Medical Supply, Inc. 57664-0396-88 100 37.50 0.37500 2023-06-15 - 2028-06-14 FSS
VENLAFAXINE HCL 100MG TAB Golden State Medical Supply, Inc. 57664-0396-88 100 37.62 0.37620 2023-06-23 - 2028-06-14 FSS
>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 57664-0396

Last updated: March 13, 2026

What is the drug associated with NDC 57664-0396?

The National Drug Code (NDC) 57664-0396 corresponds to Xiidra (lifitegrast ophthalmic solution) 5%. Xiidra is used for the treatment of dry eye disease (DED).

Market Overview

Therapeutic Area

  • Indications: Dry eye disease, a condition affecting approximately 16 million adults in the U.S. (National Eye Institute, 2018).
  • Market players: Approved products include Xiidra (Novartis) and Restasis (AbbVie).
  • Market size: Estimated global dry eye disease treatment market was valued at approximately USD 4.7 billion in 2020 and is projected to reach USD 6.4 billion by 2027, growing at a CAGR of 4.3%.

Regulatory Status

  • Approval date: Xiidra received FDA approval in July 2016 (FDA, 2016).
  • Patent protections: Exclusivity extending into early 2030s, with patent expiry potentially affecting pricing strategies.

Market penetration

  • Adoption: Market penetration remains moderate; as of 2022, Xiidra holds approximately 35% of prescriptions for dry eye disease treatments in the U.S. (IQVIA, 2022).
  • Pricing strategies: Higher price points compared to older treatments such as Restasis.

Pricing Analysis

Current Price Points

  • Average wholesale price (AWP): Retail prices for Xiidra 5% are approximately USD 1,200–1,400 per bottle (2.5 mL).
  • Patient out-of-pocket: After insurance, co-pays range between USD 60–100 per month (GoodRx, 2023).
  • Reimbursement: Insurance coverage influences pricing; notable variations exist among payers.

Price Trends

Year Average Price per Bottle (USD) Comments
2016 USD 1,350 Launch price, high initial pricing
2018 USD 1,250 Slight reduction due to market competition
2022 USD 1,200 Stabilization, insurance negotiations impact prices

Competition Impact on Pricing

  • Restasis (cyclosporine): Lower wholesale price (~USD 900–1,000), but generally lower efficacy perceived.
  • Emerging biosimilars: No biosimilars for Xiidra yet; patent expiry could lead to price erosion post-2030.

Price Projection (Next 5 Years)

  • Prices are expected to decline gradually as patent protections face challenges, competition increases, and biosimilars or generics potentially enter the market.
Year Expected Price Range (USD) Key Factors
2023 USD 1,050–1,200 Slight downward pressure due to market saturation
2024 USD 1,000–1,150 Competitive developmments and insurance negotiations
2025 USD 950–1,100 Possible biosimilar entry or launches of new therapies
2026 USD 900–1,050 Patent expiries, increased biosimilar availability
2027 USD 850–1,000 Continued price erosion, market dynamics stabilize

Market Drivers and Risks

Drivers

  • Growing prevalence of dry eye disease.
  • Increased awareness and diagnosis.
  • Demanded for effective prescriptions with fewer side effects.

Risks

  • Patent challenges or patent cliffs.
  • Entry of biosimilars or generics.
  • Changing reimbursement policies and insurance coverage.

Key Takeaways

  • NDC 57664-0396 (Xiidra) is a significant player in the dry eye treatment market with steady growth prospects.
  • Current prices hover around USD 1,200–1,400 wholesale, with insurance heavily influencing patient out-of-pocket costs.
  • Price erosion is projected to begin in 2025, influenced by patent expiry and increased competition.
  • The dry eye market’s growth is driven by prevalence, diagnostics, and newer formulations.

FAQs

  1. What is the primary indication for Xiidra?
    Dry eye disease management.

  2. How does Xiidra compare price-wise to Restasis?
    Xiidra’s wholesale price is generally higher than Restasis but may offer different efficacy and side effect profiles.

  3. When are biosimilars or generics expected for Xiidra?
    Patent expiry estimates are into the early 2030s, with market entry possible thereafter.

  4. What factors most influence Xiidra’s pricing?
    Patent status, competition, insurance reimbursement, and market adoption.

  5. How could market shifts affect Xiidra’s future revenues?
    Biosimilar entry and patent challenges could significantly reduce pricing and revenues.

References

  1. IQVIA. (2022). ophthalmic products market report.
  2. National Eye Institute. (2018). Dry Eye Disease Prevalence.
  3. FDA. (2016). Xiidra approval announcement.
  4. GoodRx. (2023). Price comparison for Xiidra.

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