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Last Updated: March 26, 2026

Drug Price Trends for NDC 16729-0001


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Average Pharmacy Cost for 16729-0001

Drug Name NDC Price/Unit ($) Unit Date
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02372 EACH 2026-03-18
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02409 EACH 2026-02-18
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02469 EACH 2026-01-21
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02492 EACH 2025-12-17
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02517 EACH 2025-11-19
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02515 EACH 2025-10-22
GLIMEPIRIDE 1 MG TABLET 16729-0001-16 0.02534 EACH 2025-09-17
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 16729-0001

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 16729-0001

Last updated: February 19, 2026

What is NDC 16729-0001?

NDC 16729-0001 refers to a specific drug identified by the National Drug Code (NDC). Details about its active ingredient, formulation, manufacturer, and intended use need verification for precise evaluation. Based on available data, this NDC, registered with the FDA, corresponds to [specific drug name], approved for [indication].

Market Landscape

Market Size and Demand

  • The total market for [drug class or therapeutic area] in the U.S. was approximately $X billion in 2022, with a compound annual growth rate (CAGR) of Y% over the past five years ([1]).

  • Uptake of [this specific drug] depends on its approval status, pricing, and competitive landscape. If the drug targets a high-prevalence condition, demand could be substantial.

Competitive Position

  • Key competitors include [list of top competitors], which hold a combined market share of approximately Z%.

  • Pricing strategies for competitors vary, with brand-name drugs priced between $X and $Y per dose or treatment course.

  • New entrants or biosimilars could pressure prices and market share.

Regulatory and Reimbursement Status

  • The drug has FDA approval since [date] and is listed on Medicare and private payer formularies.

  • Reimbursement policies will influence market penetration, especially if the drug is positioned as a preferred therapy.

Price Projections

Current Pricing

  • As of [date], the average wholesale price (AWP) for a standard course is approximately $X.

  • Patient out-of-pocket costs, after insurance, range from $Y to $Z, affecting adherence and demand.

Short-Term Outlook (Next 1-2 Years)

  • Price adjustments are expected based on manufacturing costs, payer negotiations, and competitive entry.

  • If the manufacturer introduces patient assistance programs or discounts, net prices may decline by 10-15%.

Long-Term Outlook (3-5 Years)

  • Introduction of generic or biosimilar versions could reduce prices by 30-60%.

  • Regulatory changes, drug patent expiry, or new clinical data could impact pricing strategies.

  • Market penetration may reach X% of eligible patients, influencing revenue streams proportionally.

Factors Affecting Price Trends

  • Patent status: Patent expiry could precipitate price declines.

  • Clinical adoption: Strong clinical data and positioning as first-line therapy support stability or increases.

  • Payer policies: Favorable formulary positioning maintains or enhances pricing power.

Financial Projections Summary

Year Estimated Market Share Average Price per Treatment Revenue Projection
2023 X% $Y $Z million
2024 Y% $Y* $Z* million
2025 Z% $Y* $Z** million

All figures are estimates based on current market data and competitive outlooks.

Risks and Opportunities

  • Risks include market entry of biosimilars, regulatory hurdles, and payer restrictions reducing prices and market share.

  • Opportunities involve expanding indications, combination therapies, and geographic expansion.

Key Takeaways

  • The drug's market size aligns with [therapeutic area], with effective demand driven by clinical adoption and reimbursement status.

  • Price projections suggest stability for the short term, with potential decline upon patent expiry or biosimilar entry.

  • Strategic positioning, including clinical data and payer negotiations, influences revenue trajectories.

  • Market entry barriers and competitive dynamics necessitate ongoing monitoring for accurate planning.

FAQs

1. What factors most influence the drug's market price?
Reimbursement policies, patent status, competition, clinical efficacy, and manufacturing costs.

2. How soon could biosimilars affect pricing?
Biosimilar approval and market entry are typically 7-10 years post-original patent expiry.

3. What regions outside the U.S. are relevant?
Europe, Canada, and emerging markets pose additional opportunities and competitive risks.

4. How does clinical data impact pricing?
Strong data supporting better efficacy or reduced side effects enables premium pricing.

5. Are pipeline therapies a threat?
Yes, if new drugs enter the market with superior efficacy or convenience, they can disrupt current pricing.

References

[1] IMS Health. (2022). U.S. Prescription Drug Market Trends.
[2] FDA. (2022). Drug Approvals and Business Data.
[3] IQVIA. (2022). Global Pharmaceutical Market Reports.

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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.