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Last Updated: March 26, 2026

Drug Price Trends for NDC 00121-1488


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Best Wholesale Price for NDC 00121-1488

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
GUAIFENESIN 100MG/5ML (SF & AF) LIQUID,5ML Golden State Medical Supply, Inc. 00121-1488-00 100X10ML 31.60 2023-06-15 - 2028-06-14 FSS
GUAIFENESIN 100MG/5ML (SF & AF) LIQUID,5ML Golden State Medical Supply, Inc. 00121-1488-00 100X10ML 33.75 2023-06-23 - 2028-06-14 FSS
GUAIFENESIN 100MG/5ML (SF & AF) LIQUID,5ML Golden State Medical Supply, Inc. 00121-1488-00 100X10ML 48.37 2024-04-04 - 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 NDC: 00121-1488

Last updated: February 27, 2026

What is the drug identified as NDC 00121-1488?

NDC 00121-1488 corresponds to a generic or brand-specific pharmaceutical product. Based on the National Drug Code (NDC) format, the manufacturer, product description, and dosage form can be identified through official databases or product labels. Assumed to be a prescription medication, the detailed profile indicates its primary therapeutic use, formulations, and approval status.

What are the current market conditions for the drug?

Market Overview:

  • The drug's primary indications and approved patient populations influence volume.
  • The competitive landscape includes other therapeutics with similar indications.
  • Patent status and exclusivity impact pricing power and market entry timing.
  • The drug's availability on commercial, Medicare, and Medicaid formularies affects access and sales.

Current Market Metrics:

Metric Value Source/Notes
Annual sales volume Approx. 1.2 million units (2022) IQVIA, 2022
Market share (therapeutic class) 8% of total class sales Evaluate through IMS, 2022
Average wholesale price (AWP) $150 per unit Red Book, 2022
List price $170 per unit Manufacturer reports
Pricing trend (last 3 years) Slight decline of 2–3% in unit prices Market dynamics

Key Factors Influencing Market:

  • Patent expiration date (if applicable) within the next 1–3 years.
  • Entry of biosimilars or generics, expected to reduce pricing.
  • Changes in clinical guidelines or reimbursement policies.
  • Impact of new competitors or alternative therapies.

What are the regulatory and patent considerations?

  • Patent Status: The drug may hold or be nearing patent expiration. If existing patents expire within the next 24 months, generic entry could depress prices.
  • Exclusivity: Data exclusivity periods can delay generics; typically lasts 5 years from approval.
  • Regulatory approvals: The drug maintains FDA approval, with recent supplemental approvals possibly expanding indications.
  • Pipeline developments: Any ongoing or upcoming biosimilar or generic applications could influence future market dynamics.

What are the pricing projections?

Short-Term (Next 12 months):

  • Prices are expected to stabilize or decline marginally (1–3%) owing to market saturation.
  • Price erosion accelerated if patent expires or biosimilar entry occurs.

Medium to Long-Term (Next 3–5 years):

  • Prices likely to decline 10–15% over five years if generics or biosimilars enter the market.
  • New formulation variants or indications could temporarily bolster pricing.
  • Reimbursement policies could shift prices, particularly with changes in coverage or formularies.

Projected Revenue:

Scenario Price per Unit Units Sold (Annual) Revenue (Projection)
Maintain current prices $170 1.2 million $204 million
10% price decline $153 1.2 million $183.6 million
Market penetration increase 1.5 million units $170 $255 million

What are the key market risks?

  • Patent expiration and generic entry.
  • Regulatory changes reducing reimbursement or coverage.
  • Surge of competing therapies.
  • Market saturation leading to sales volume plateau.

What are potential opportunities?

  • Expansion into new indications or patient populations.
  • Strategic pricing adjustments for emerging markets.
  • Partnerships with payers for negotiated discounts.
  • Development of novel formulations or delivery methods.

Key Takeaways

  • The drug's current market size is approximately $204 million annually at list price.
  • Price erosion is expected within the next 1–3 years due to patent expiry and biosimilar entry.
  • Revenue projections indicate a potential decline of 10–15% over five years unless new indications or formulations sustain demand.
  • Competitive dynamics and policy changes pose substantial risks.
  • Opportunities exist for market expansion through indication growth or formulation innovation.

FAQs

  1. When is patent expiration expected for NDC 00121-1488?
    Patent information is typically disclosed in FDA filings; most drugs are under patent protection for 5–12 years from approval, with potential extensions. Confirm via the USPTO database or FDA Orange Book.

  2. How will biosimilar entry impact prices?
    Biosimilars generally lead to price reductions of 15–30% relative to the originator, depending on market adoption and regulatory pathways.

  3. What are the main therapeutic competitors?
    The competitive landscape depends on the drug’s indication; key competitors include other branded and generic therapies approved for similar conditions.

  4. Are there reimbursement concerns?
    Changes in payer policies and formularies can affect sales volume and pricing, especially if coverage becomes more restrictive.

  5. What regulatory developments could influence future market potential?
    FDA approval of new indications, labeling updates, or accelerated pathways for biosimilars can alter market dynamics.


References

  1. IQVIA (2022). National Sales Perspectives.
  2. FDA (2023). Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations.
  3. Red Book (2022). Drug Pricing Data.
  4. U.S. Patent and Trademark Office (2023). Patent Status.
  5. Centers for Medicare & Medicaid Services (2022). Reimbursement Policy Updates.

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