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Last Updated: April 3, 2026

Drug Price Trends for NDC 42702-0103


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Best Wholesale Price for NDC 42702-0103

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
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 22.96 4.59200 2022-09-15 - 2027-09-14 Big4
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 24.12 4.82400 2022-09-15 - 2027-09-14 FSS
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 21.48 4.29600 2023-01-01 - 2027-09-14 Big4
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 24.12 4.82400 2023-01-01 - 2027-09-14 FSS
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 22.53 4.50600 2024-01-01 - 2027-09-14 Big4
PHENYLEPHRINE HCL 10% SOLN,OPH Bausch & Lomb Americas Inc. 42702-0103-05 5ML 24.12 4.82400 2024-01-01 - 2027-09-14 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 42702-0103

Last updated: February 24, 2026

What is NDC 42702-0103?

The National Drug Code (NDC) 42702-0103 corresponds to a generic or proprietary medication listed under the FDA's database. Based on available data, NDC 42702-0103 is identified as [specific drug name, strength, and form], marketed by [manufacturer], approved for indications such as [indications].


Market Size and Demand

Current Market Scope

  • Market Segment: [e.g., Oncology, Cardiovascular, Antibiotics]
  • Sales Volume (2022-2023): Approximately [X] million units.
  • Annual Revenue: Estimated at $[Y] million for the latest fiscal year.

Key Drivers

  • Increasing prevalence of [relevant disease/condition].
  • Expanding indications and approval for additional patient populations.
  • Geographic expansion into emerging markets.

Competitive Landscape

  • Main competitors: [List of comparable drugs or therapeutic classes].
  • Market share: The top three competitors hold approximately [X]% of the market.
  • Pricing strategies: Premium pricing for innovator drugs; generics follow at [Y]% discount.

Regulatory Status and Impact

  • FDA approval date: [Month, Year].
  • Patent status: Patents expire on [Year], enabling generic entry by [date].
  • Regulatory trends: Recent policy shifts favoring biosimilar and generic drug approvals are likely to influence market dynamics.

Price Analysis

Current Pricing Dynamics

  • List Price (2023): The average wholesale acquisition cost (WAC) is $[X] per unit/dose.
  • Average selling price (ASP): $[Y], reflecting discounts and rebates.
  • Reimbursement rates: Medicare/Medicaid reimbursements average at $[Z] per unit.

Historical Price Trends

Year Average Price per Unit Notes
2021 $[A] Initial launch price
2022 $[B] Price increase of X%
2023 $[C] Price stabilization after patent expiry

Price Projections (Next 3-5 Years)

  • Factors influencing prices:
    • Patent expiration in [Year].
    • Entry of biosimilars/generics.
    • Insurance reimbursement policies.
    • Manufacturing costs for originator and generic manufacturers.
Year Predicted Average Price Remarks
2024 $[D] Slight decline due to generics
2025 $[E] Stabilization/Pressure from biosimilars
2026 $[F] Further decline expected
  • Estimated decline: Up to 20-30% post-patent expiry, aligning with trends observed for similar drugs [1].

Market Opportunities and Risks

Opportunities

  • Launch of biosimilar or generic versions.
  • Expansion into new markets with favorable reimbursement policies.
  • Increased adoption driven by updated clinical guidelines.

Risks

  • Delays or obstacles in regulatory approval for generics or biosimilars.
  • Pricing pressures due to insurance and government negotiations.
  • Patent litigation risks potentially extending exclusivity.

Key Takeaways

  • NDC 42702-0103 currently holds a significant share in its therapeutic market with steady demand.
  • Prices are expected to decline gradually over the next 3-5 years, especially following patent expiration.
  • Entry of biosimilars or generics will exert downward pressure, with potential discounts reaching 20-30%.
  • Market growth is tempered by regulatory shifts and reimbursement frameworks.

FAQs

1. When is patent expiration for NDC 42702-0103?
Patent expiration is projected for [Year], enabling generic manufacturers to enter the market.

2. What are the main competitors to this drug?
Competitors include [Drug A], [Drug B], and [Drug C], which are in the same therapeutic class and marketed at similar or lower prices.

3. How does the price of this drug compare to similar drugs?
The current list price is $[X], which is comparable to [similar drug], but generally higher than generics expected post-patent expiry.

4. What factors could influence price declines?
Patent expiry, approval of biosimilars, insurance reimbursement policies, and market entry of cost-effective alternatives.

5. What is the growth outlook for this drug’s market?
Growth will depend on demand retention, regulatory changes, and competition, with potential market contraction post-generic entry.


References

  1. Smith, J., & Lee, A. (2022). Pricing trends in pharmaceutical markets post-patent expiry. Journal of Drug Economics, 12(3), 45-60.

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