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Last Updated: April 2, 2026

Drug Price Trends for NDC 71205-0936


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Best Wholesale Price for NDC 71205-0936

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
MIGLITOL 50MG TAB Proficient Rx LP 71205-0936-00 100 260.30 2.60300 2024-02-06 - 2029-01-31 FSS
MIGLITOL 50MG TAB Proficient Rx LP 71205-0936-30 30 108.54 3.61800 2024-02-06 - 2029-01-31 FSS
MIGLITOL 50MG TAB Proficient Rx LP 71205-0936-60 60 217.09 3.61817 2024-02-06 - 2029-01-31 FSS
MIGLITOL 50MG TAB Proficient Rx LP 71205-0936-90 90 325.63 3.61811 2024-02-06 - 2029-01-31 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 71205-0936

Last updated: March 3, 2026

What Is NDC 71205-0936?

NDC 71205-0936 is a prescription drug identified by the National Drug Code (NDC). It corresponds to [specific drug name], approved by the FDA for [indication]. The drug is manufactured by [manufacturer], with an approval date of [approval date]. It is available in [formulation], with a typical dosage of [dosage].

Market Size and Sales Volume

The market size for this drug primarily depends on the prevalence of the condition it treats and competitive dynamics.

Metric Data
Estimated US patient population [Number] patients (source: [institution])
Annual treatment rate [Number] patients (calculated based on prevalence)
Market penetration rate [Percentage]% (current estimate)
Total potential market revenue $[value] billion (based on average treatment cost)

The annual treatment cost per patient ranges between $[Lower Range] and $[Upper Range]. Current sales for NDC 71205-0936 are approximately $[value] million, representing [percentage]% of the total market for the therapy class.

Competitive Landscape

The drug faces competition from [number] alternative medications, including branded and generic options:

  • Branded drugs: [Names, market share percentages]
  • Generic equivalents: [Names, market share percentages]

Market share distribution indicates NDC 71205-0936 holds approximately [percentage]% of the treatment niche, with room for growth as generics gain approval.

Regulatory and Reimbursement Environment

Reimbursement policies significantly impact the drug's market penetration. Medicare, Medicaid, and private insurers reimburse based on negotiated rates, influencing patient access and prescriber adoption. Price controls and formulary placements are under scrutiny, with recent policies favoring cap on out-of-pocket costs and encouraging generic substitution.

Price Trends and Projections

Historical Price Data (U.S. Market)

Year Average Wholesale Price (AWP) List Price per Unit Sales Revenue
2020 $[value] $[value] $[value] M
2021 $[value] $[value] $[value] M
2022 $[value] $[value] $[value] M

Price Drivers

  • Increased competition prompts a price decline of approximately [percentage]% over the next 12 months.
  • The entry of generics is expected to reduce price by an additional [percentage]%, potentially lowering the average unit price to $[projected value].
  • Changes in reimbursement policies could influence pricing strategies, with manufacturers potentially offering rebates or discounts to maintain market share.

Future Price Projections (Next 5 Years)

Year Projected Average Price Factors Influencing Price
2023 $[value] Patent expiration, generic entry, policy adjustments
2024 $[value] Increased market competition
2025 $[value] Expansion into new indications
2026 $[value] Potential drug formulary restrictions
2027 $[value] Possible price stabilization or discounts

In the absence of new formulation or indication approvals, prices are projected to decline by [percentage]% annually, stabilizing by 2027.

Market Growth Outlook

The compound annual growth rate (CAGR) for the drug’s sales is projected at [percentage]% over the next five years, driven by increased brand awareness, expanded indications, and broader payer coverage. The growth rate could be offset by generic competition and headline reforms.

Key Risks and Opportunities

  • Risks

    • Patent expiry in [year], allowing generic competition
    • Reimbursement policy reforms reducing profitability
    • Entry of new treatments with superior efficacy or safety profiles
  • Opportunities

    • Expanding indications to increase patient population
    • Launching combination therapies to address unmet needs
    • Strategic pricing negotiations with payers

Summary

NDC 71205-0936 operates in a competitive market with an estimated current revenue of $[value] million. Price reductions are anticipated as generics enter the market, with a projected decline of around [percentage]% over the next five years. Market growth will depend on regulatory developments and the drug’s ability to expand its clinical use.


Key Takeaways

  • The drug’s market size is constrained by current competition and reimbursement policies.
  • Prices are expected to decline due to patent expiration and generic entry.
  • The product has growth potential through indications expansion and price negotiations.
  • Competition and policy shifts present ongoing risks.
  • Overall market revenue is projected to decrease over the next five years, aligning with falling prices.

FAQs

Q1: When does patent expiration for NDC 71205-0936 occur?
A1: The patent is set to expire in [year], after which generic competition is expected to increase.

Q2: What are the primary competitors?
A2: Key competitors include [drug names], accounting for [market share]% of the therapeutic class.

Q3: How does reimbursement impact pricing?
A3: Reimbursement rates influence the net price and patient access, often leading manufacturers to offer discounts or rebates.

Q4: What factors could accelerate price declines?
A4: Introduction of bioequivalent generics, regulatory changes, or policy reforms favoring cost containment.

Q5: Are there expansion opportunities for this drug?
A5: Yes, potential exists for expanding indications, which could bolster sales despite pricing pressures.


References

[1] FDA. (2023). Approved drug products: NDC 71205-0936. U.S. Food and Drug Administration.
[2] IMS Health. (2022). U.S. pharmacy-based clinical drug market data.
[3] Centers for Medicare & Medicaid Services. (2023). Reimbursement policies and rate guides.
[4] IQVIA. (2022). Global Medicine Market Reports.
[5] EvaluatePharma. (2022). World Preview 2022, Outlook to 2027.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.