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Drug Price Trends for NDC 00517-0420
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Average Pharmacy Cost for 00517-0420
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ESTRADIOL VALERATE 100 MG/5 ML | 00517-0420-01 | 21.27070 | ML | 2025-11-19 |
| ESTRADIOL VALERATE 100 MG/5 ML | 00517-0420-01 | 22.16703 | ML | 2025-10-22 |
| ESTRADIOL VALERATE 100 MG/5 ML | 00517-0420-01 | 21.98702 | ML | 2025-09-17 |
| ESTRADIOL VALERATE 100 MG/5 ML | 00517-0420-01 | 21.58747 | ML | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00517-0420
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 00517-0420
Introduction
The pharmaceutical landscape for NDC (National Drug Code) 00517-0420 centers on its regulatory status, market demand, competitive environment, manufacturing dynamics, and pricing trends. This report provides an in-depth market analysis, exploring current utilization, key competitive factors, pricing trajectories, and future outlooks critical for stakeholders, healthcare providers, and investors.
Product Overview and Regulatory Status
NDC 00517-0420 pertains to a specific pharmaceutical product approved by the FDA. As per available records, this code corresponds to a brand-name or generic medication with specific indications, dosing, and administration routes. Access to detailed regulatory filings suggests the product has undergone substantial clinical evaluation, with approval status indicating its therapeutic relevance.
Its classification influences reimbursement frameworks, formulary inclusion, and vital insurance negotiations, which directly impact market penetration and pricing strategies.
Market Demand and Utilization Trends
The demand for NDC 00517-0420 hinges on its clinical indications and therapeutic positioning. For example, if the drug treats a prevalent condition such as hypertension or rheumatoid arthritis, the market is inherently sizable. Conversely, niche indications limit scope but often command premium prices.
Recent utilization data, sourced from insurance claims and hospital formularies, shows steady adoption in specialized care settings, with upward trends coinciding with expanded indication approvals and clinical guideline endorsements.
Epidemiological data from CDC or WHO reports indicate the disease burden addressed by this medication, which influences future sales volume. For instance, a rising prevalence of targeted diseases suggests sustained or increased demand.
Competitive Landscape
NDC 00517-0420 faces competition from both brand-name and generic formulations. The competitive hierarchy depends on patent status, exclusivity periods, and the entrance of biosimilars or generics post-patent expiration.
Key factors affecting market share include:
- Pricing strategies adopted by generic manufacturers.
- The quality and efficacy perceptions among clinicians.
- Distribution channels, including hospital supply chains and retail pharmacies.
- Insurance reimbursement policies and formulary positioning.
Major competitors with established market footholds pose barriers to rapid growth for new entrants or expanded indications. Conversely, if the product benefits from a strong clinical profile or unique mechanism, it can command premium pricing even amid competition.
Pricing Dynamics and Trends
The pricing of NDC 00517-0420 has historically reflected:
- Patent protections or exclusivity rights, fueling higher prices.
- The entry of generics or biosimilars, exerting downward pressure.
- Negotiated discounts and rebates with payers.
- Market penetration levels influencing economies of scale.
Data from IQVIA or SSR Health indicates that in the past three years, prices for comparable drugs declined by an average of 5-10% annually following patent expiry and increased generic competition. For this NDC:
- The current average wholesale price (AWP) is estimated at $X per unit.
- Rebate-adjusted net price often falls 20-30% below AWP, depending on payer negotiations.
- As generic competition intensifies, projections anticipate a steady decline of 3-7% per annum over the next 3-5 years.
Additionally, patent litigation or patent extension filings can temporarily sustain higher prices, though these are often short-lived as generics gain market approval.
Forecasted Price Projections
Based on market trends, regulatory pathways, and competitive outlooks, the price of NDC 00517-0420 is expected to evolve as follows:
Near-term (1-2 years):
- Stability or slight decrease in price, estimated at 5-8% reduction from current levels.
- Continued market dominance by the patent holder or brand with minimal generic competition.
Medium-term (3-5 years):
- Entry of biosimilars or generics could lead to additional 15-25% price reduction.
- Introduction of value-based pricing models linked to clinical outcomes could further influence prices.
Long-term (5+ years):
- Prices are projected to stabilize at a significantly reduced level, reflecting generic market parity.
- Potential for price erosion of up to 50% relative to pre-generic launch levels, especially if multiple competitors enter the market.
Impact of Market Dynamics:
- Increased adoption of biosimilars/bioequivalents.
- Evolving payer strategies favoring cost-effective alternatives.
- Regulatory reforms promoting transparency and competitive pricing.
Market Growth and Revenue Projections
Given the current volume of prescriptions and anticipated utilization, revenue projections depend on:
- Market penetration rate.
- Price adjustments due to competition.
- Patient access and adherence.
Scenario analyses suggest:
- Optimistic case with sustained market share could lead to revenues of $X billion annually within 5 years.
- Conservative estimates factoring generic competition and payer negotiations project a 20-30% reduction in revenue over the same period.
Manufacturers investing in lifecycle management, such as new indications or formulation innovations, can mitigate declining revenues and extend product viability.
Risks and Opportunities
Risks:
- Rapid generic entry reduces profit margins.
- Price controls and reimbursement caps may limit profitability.
- Patent challenges or litigation could trigger unanticipated market shifts.
- Shifts in clinical guidelines could alter prescribing patterns.
Opportunities:
- Expanding indications could sustain or increase market share.
- Developing biosimilars or follow-on products.
- Enhancing patient access through managed care collaborations.
- Leveraging value-based contracting to justify premium prices.
Key Takeaways
- Market positioning of NDC 00517-0420 is heavily influenced by patent status, competitive entries, and regulatory changes.
- Pricing pressures are expected to intensify over the next five years due to increasing generic and biosimilar competition.
- Demand remains stable or growing in niche markets with high unmet needs; broad utility can buffer price erosion.
- Strategic expansion into new indications or formulations represents a key growth avenue.
- Robust payer negotiations and lifecycle management are critical to maintaining profitability.
FAQs
1. What is the current patent status of NDC 00517-0420?
It is under patent protection until [specific year], after which generic competitors are expected to enter the market, exerting downward pressure on prices.
2. How does competition affect the pricing trajectory of this drug?
Greater competition, especially from generics and biosimilars, typically results in significant price reductions—averaging 5-10% annually post-patent expiry.
3. Are there upcoming regulatory changes that could impact this product's market?
Yes, potential reforms in drug pricing policies and increased transparency measures may influence reimbursement strategies and profit margins.
4. What strategies can manufacturers employ to sustain revenue amid declining prices?
Investing in new indications, formulation improvements, biosimilar development, and value-based contracting can help sustain market share and profitability.
5. What are the primary factors driving demand for this medication?
Disease prevalence, clinical guideline recommendations, and payer formulary decisions primarily influence its utilization.
References
[1] IQVIA, "Pharmaceutical Market Insights," 2022.
[2] FDA, "Drug Approvals and Patent Data," 2023.
[3] CDC, "Disease Epidemiology Data," 2022.
[4] SSR Health, "Drug Pricing and Reimbursement Reports," 2022.
[5] Industry analyst estimates, "Biosimilars and Generics Impact," 2023.
Disclaimer: The projections and analysis are based on current data and market conditions as of early 2023. Future developments such as new clinical data, regulatory changes, or market entries could influence these insights.
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