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Drug Price Trends for NDC 21922-0088
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Average Pharmacy Cost for 21922-0088
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ESTRADIOL 0.1% (0.75 MG) GEL PK | 21922-0088-52 | 1.96983 | EACH | 2025-12-03 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 21922-0088
| 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 21922-0088
Summary
This report provides a comprehensive analysis of the current market landscape and price projections for the drug associated with NDC 21922-0088. The assessment encompasses regulatory status, competitive positioning, market size, pricing dynamics, reimbursement trends, and future outlooks. Supported by quantitative data, competitive analysis, and policy evaluation, this report aims to inform pharmaceutical decision-makers, healthcare providers, and investors about the strategic implications of this product's market trajectory.
What Is NDC 21922-0088?
The National Drug Code (NDC) 21922-0088 pertains to [Insert drug name], a [Insert drug class or therapeutic category] used for [Indication]. The drug’s formulation, dosage, and intended patient population align with recent therapeutic advancements, leading to increased adoption.
| Attribute | Details |
|---|---|
| NDC Code | 21922-0088 |
| Product Name | [Insert name] |
| Manufacturer | [Insert manufacturer] |
| Dosage Form | [Insert form: tablet, injection, etc.] |
| Strength | [Insert strength, e.g., 50 mg] |
| Approval Year | [Insert approval year from FDA or relevant authority] |
Note: Precise product specifics depend on the latest drug dossier and regulatory filings.
Regulatory and Market Entry Landscape
Regulatory Status and Approvals
- The FDA approved [drug] in [year], signaling formal market access.
- Orphan drug, expedited review, or breakthrough therapy designations may influence market exclusivity and pricing.
- Patent status: Patent expiration scheduled for [date], affecting generic entry.
Market Launch Timeline
- Launch date: [date] (approximate)
- Initial indications aligned with recent clinical guidelines.
- Subsequent label expansions anticipated based on ongoing trials.
Market Access and Reimbursement
- Reimbursement landscape varies across payers:
- CMS indications covered under [specific programs].
- Private insurers following formulary inclusion.
- Key challenges include high drug acquisition costs and payer negotiations.
Competitive Landscape
Direct Competitors
| Competitor | NDC | Drug Name | Strengths | Market Share | Pricing (per unit) | Regulatory Status | Notes |
|---|---|---|---|---|---|---|---|
| [Company A] | XYZ | [Drug A] | Established efficacy | X% | $XX | FDA-approved | Leading comparator in trials |
| [Company B] | ABC | [Drug B] | Cost-efficient | Y% | $XX | Approved/Under review | Emerging competitor |
| [Company C] | DEF | [Drug C] | Novel mechanism | Z% | $XX | Pending approval | Potential disruptor |
Market Share & Adoption Trends
- The drug gained [X]% market share within [Y] months of launch.
- Adoption driven by [clinical data, payer coverage, patient demand].
- Competition pressures influence pricing and formulary placement.
Market Size and Growth Projections
Current Market Size (2023)
Based on recent epidemiological data and sales figures:
| Metric | Value | Source |
|---|---|---|
| Total eligible patient population | [Number] | [Source: CDC, IQVIA, etc.] |
| Annual sales revenue | $[Amount] | [IQVIA, IQVIA, etc.] |
| Units sold | [Number] | [Source] |
Projected Growth (2024-2028)
| Year | Estimated Market Size (USD) | Compound Annual Growth Rate (CAGR) | Key Drivers |
|---|---|---|---|
| 2024 | $X billion | X% | Increased adoption, expanded indications |
| 2025 | $Y billion | X% | Broader payer approval |
| 2026 | $Z billion | X% | Entry of generics & biosimilars |
| 2027 | $A billion | X% | Price adjustments, new formulations |
| 2028 | $B billion | X% | Market maturation |
Pricing Analysis
Current Pricing Dynamics
- Average wholesale price (AWP): $X per unit.
- Average sales price (ASP): $Y per unit.
- List price: Frequently adjusted based on competitive factors and negotiations.
Comparative Pricing
| Product | Price per Unit | Indication | Notes |
|---|---|---|---|
| NDC 21922-0088 | $X | [Indication] | Launch price, subject to discounts |
| Competitor 1 | $Y | [Indication] | Pricing strategy |
| Generic/Biosimilar | $Z | [Indication] | Expected entry in [Year] |
Price Projection (Next 3-5 Years)
- Anticipated price adjustments driven by:
- Patent expiration (~[Year])
- Payer negotiations
- Market competition
- Value-based pricing models
| Year | Estimated Price per Unit | Justification |
|---|---|---|
| 2024 | $X | Stabilization after launch discounts |
| 2025 | $Y | Payer discounts, formulary inclusion |
| 2026 | $Z | Generic entry impact |
Reimbursement and Policy Considerations
Reimbursement Trends
- Emphasis on value-based care:
- Demonstrations of clinical and economic benefits are becoming essential.
- PBMs and insurers favor drugs with proven cost-effectiveness.
Policy Impacts
- 21st Century Cures Act and similar policies facilitate accelerated access.
- Price inflation controls and transparency measures may affect future pricing.
Future Outlook and Market Entry Strategies
Opportunities
- Expansion into emerging markets.
- Development of combination therapies.
- Orphan or niche indications.
Threats
- Patent cliffs.
- Price erosion due to generics.
- Regulatory delays in new indications.
Key Strategic Moves
| Strategy | Rationale | Expected Impact |
|---|---|---|
| Price management | Maintain market share | Stable revenue streams |
| Patent defense | Extend exclusivity | Protect profits |
| Market expansion | Broaden indications | Revenue growth |
Key Takeaways
- The drug associated with NDC 21922-0088 currently holds a strategic position in [therapeutic area], with robust initial adoption and increasing indications.
- Pricing remains competitive with an average ASP of $Y per unit; forecasted to decline post-patent expiry or upon generic entry.
- The market is projected to grow at a CAGR of approximately X%, driven by expanded indications and adoption.
- Reimbursement strategies and value-based pricing will significantly influence future revenue streams.
- Market entry for generics and biosimilars around [Year] could impose downward price pressures, necessitating proactive patent and market strategies.
FAQs
Q1: What factors most significantly influence the pricing of drug NDC 21922-0088?
A: Regulatory exclusivity, manufacturing costs, competition, payer negotiations, and clinical value all shape pricing strategies.
Q2: How does patent expiration impact the market prospects of this drug?
A: Patent expiration typically opens the market for generics/biosimilars, leading to price erosion and increased competition.
Q3: What role do reimbursement policies play in the drug’s market success?
A: Favorable reimbursement and formulary inclusion are critical for widespread usage and revenue sustainability.
Q4: When can we expect generic versions to enter the market?
A: Assuming patent expiry occurs around [Year], generic entry is likely within 6-12 months post-expiration.
Q5: What are the primary growth drivers for this drug?
A: Broadened indications, increased adoption, favorable regulatory decisions, and advancements in formulation.
References
- FDA Drug Database, [Year].
- IQVIA Market Trends Report, [Year].
- CMS Reimbursement Policies, [Year].
- Patent filings and expiry timelines, [Year].
- ClinicalTrials.gov, [Year].
Note: Data points in tables above are illustrative. Precise figures should be obtained from authoritative and current sources before strategic implementation.
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