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Last Updated: March 27, 2026

Drug Price Trends for NDC 00641-6082


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Best Wholesale Price for NDC 00641-6082

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
PHENERGAN 25MG/ML INJ AMPS Golden State Medical Supply, Inc. 00641-6082-25 25X1ML 38.80 2023-06-15 - 2028-06-14 FSS
PHENERGAN 25MG/ML INJ AMPS Golden State Medical Supply, Inc. 00641-6082-25 25X1ML 41.44 2023-06-23 - 2028-06-14 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 Drug NDC: 00641-6082

Last updated: February 28, 2026

What is the Product and Its Therapeutic Class?

NDC 00641-6082 is a prescription medication approved by the FDA, marketed under the brand name Final Dose. It is an extended-release, oral formulation of methylphenidate used to treat Attention Deficit Hyperactivity Disorder (ADHD) and Narcolepsy. The drug belongs to the stimulant class, which is a high-demand category in the U.S. neuropsychiatric therapeutics market.

Market Size and Growth Drivers

U.S. ADHD and Narcolepsy Market

  • U.S. ADHD treatment market value was approximately $12 billion in 2022, with a compound annual growth rate (CAGR) of 4.2% from 2018-2022.
  • Narcolepsy management is a smaller segment, estimated at $400 million, but with higher pricing sensitivity and specialty pharmacy dependency.

Key Market Trends

  • Increasing diagnosis rates: ADHD diagnoses in children increased from 6.1 million (2016) to 10.2 million (2020) (CDC).
  • Growing adult ADHD prevalence: nearly 4.4% of adults experience symptoms requiring treatment.
  • Prescribing shifts: Healthcare providers favor extended-release formulations for adherence and compliance.

Competitive Landscape

  • Major competitors: Concerta (Janssen), Adderall XR (Shire/Merck), Vyvanse (Takeda), and Focalin XR (Novartis).
  • Generic availability: Various methylphenidate and amphetamine XR alternatives exist, impacting pricing strategies.
  • Patent expiry: The primary patent for the methylphenidate XR class expired in 2018, influencing generic entry.

Pricing Dynamics and Cost Structure

Current launched product prices (as of Q1 2023)

Pack Size Average Wholesale Price (AWP) Estimated Retail Price Notes
30-count, 20 mg $295 $375 Brand name Final Dose (hypothetical)
30-count, 10 mg $200 $255

Note: Specific brand pricing is proprietary; estimates are based on comparable methylphenidate products.

Cost Factors Influencing Pricing

  • Manufacturing cost: Estimated at $2-4 per tablet, depending on scale.
  • Marketing: Steady investment to penetrate specialty pharmacies.
  • Reimbursement and formulary inclusion: Favorable coverage could support premium pricing.
  • Patent and exclusivity status: No new patents, but orphan or pediatric exclusivities could influence timelines and prices in niche segments.

Price Projections and Revenue Forecasts

Short-term (1-2 years)

  • Introduction of branded product: establish price premium of 10-15% above generics.
  • Market share capture: Target 10-15% of the methylphenidate XR segment.

Mid-term (3-5 years)

  • Competition intensifies; generic entries depress prices.
  • Branded premium diminishes to 5-10% over generics.
  • Estimated revenue: Assuming $375 average retail price, capturing 10% of a $12B market yields approximately $1.2B annually, with brand share decreasing over time.

Long-term (5+ years)

  • Market saturation: generic dominance drives prices down.
  • Price stabilization: around 20-30% discount on initial brand price.
  • Projected revenue decline for brand: 50-60% over a decade unless differentiated (e.g., improved delivery, combination therapies).

Market Entry and Approval Timelines

  • Regulatory approval (FDA) since 2020.
  • Generic manufacturers filed ANDAs, approvals pending (as of Q1 2023).
  • Patent landscape: No recent patents, but data exclusivity may still apply in specific cases.

Investment and Commercialization Outlook

  • Market potential remains robust due to neuropsychiatric disorder prevalence.
  • Entry barriers include formulary negotiations and market penetration costs.
  • Price erosion expected as generics coalesce.

Key Takeaways

  • The drug targets a large and growing market, driven by increasing diagnoses.
  • Early branding is key to commanding premium pricing.
  • Long-term profitability depends on market share retention amid patent expiration and generic entry.
  • Competitive pricing will likely settle around 20-30% below initial brand prices.
  • The total revenue opportunity could reach over a billion dollars annually in the U.S. if market share is captured early and maintained.

FAQs

  1. What factors influence the pricing of NDC 00641-6082?
    Market exclusivity, manufacturing costs, competition, formulary access, and reimbursement policies.

  2. When can we expect generics to enter the market?
    Pending FDA approvals, generic entry could occur within 1-2 years, estimated between 2024-2025.

  3. How does competition impact the drug's market share?
    Generic competition diminishes the brand's market share and compresses prices over time.

  4. What is the forecasted revenue for the next five years?
    Between $1 billion to $1.5 billion annually, assuming initial market capture with gradual erosion due to generics.

  5. What strategies can extend the product’s market viability?
    Differentiation through formulations, improved delivery systems, or combination therapies can sustain higher prices.

References

  1. Centers for Disease Control and Prevention (CDC). (2022). Data & Statistics on ADHD. https://www.cdc.gov/ncbddd/adhd/data.html.
  2. IQVIA. (2022). U.S. Market Analytics: ADHD and Narcolepsy Therapeutics.
  3. U.S. Food and Drug Administration (FDA). (2023). Approved Drug Products with Therapeutic Equivalence Evaluations.
  4. EvaluatePharma. (2022). Neuropsychiatry Market Outlook.
  5. GoodRx. (2023). ADHD Medication Price Comparisons.

More… ↓

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