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Drug Price Trends for NDC 00904-7382
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Average Pharmacy Cost for 00904-7382
Drug Name | NDC | Price/Unit ($) | Unit | Date |
---|---|---|---|---|
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.17801 | EACH | 2025-07-23 |
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.18471 | EACH | 2025-06-18 |
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.19893 | EACH | 2025-05-21 |
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.21726 | EACH | 2025-04-23 |
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.23067 | EACH | 2025-03-19 |
PROCHLORPERAZINE 10 MG TAB | 00904-7382-06 | 0.21092 | EACH | 2025-02-19 |
>Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 00904-7382
Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
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>Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for Tadalafil (NDC: 00904-7382)
Tadalafil, identified by NDC code 00904-7382, is a phosphodiesterase type 5 (PDE5) inhibitor primarily used to treat erectile dysfunction (ED) and benign prostatic hyperplasia (BPH). Marketed as a generic equivalent to Cialis, this formulation—typically 5 mg tablets manufactured by Teva Pharmaceuticals—has seen steady demand amid an aging global population and increasing awareness of men's health issues. This analysis examines the current market dynamics, competitive landscape, and price projections for NDC 00904-7382, drawing on industry data to provide actionable insights for stakeholders in pharmaceuticals, healthcare providers, and investors.
Overview of Tadalafil and NDC 00904-7382
NDC 00904-7382 represents Teva's generic Tadalafil 5 mg tablets, approved by the FDA in 2018 following the expiration of Eli Lilly's original patent for Cialis [1]. As a once-daily treatment option, it addresses ED in approximately 30 million men in the U.S. alone, according to the National Institutes of Health [2]. The drug's market appeal stems from its efficacy, longer half-life compared to competitors like Sildenafil, and cost-effectiveness as a generic. Global sales of Tadalafil generics reached $1.2 billion in 2023, driven by rising prescriptions in North America and Europe, where ED prevalence is projected to grow at a 5% compound annual growth rate (CAGR) through 2030 [3].
The U.S. market for ED treatments, including NDC 00904-7382, benefits from broad insurance coverage and telemedicine adoption, which surged during the COVID-19 pandemic. Teva holds a significant share in the generic segment, with production scaled through partnerships in India and Europe to meet demand. However, supply chain disruptions, such as those from raw material shortages, have occasionally impacted availability, as reported in IQVIA's 2023 pharmaceutical supply chain analysis [4].
Current Market Analysis
The market for Tadalafil (NDC: 00904-7382) operates within a mature ED therapeutics sector valued at $4.5 billion globally in 2023 [3]. In the U.S., generics like this one dominate, accounting for 85% of Tadalafil prescriptions, per FDA data [1]. Demand factors include an aging demographic—men over 50 represent 70% of users—and lifestyle influences such as diabetes and hypertension, which exacerbate ED [2]. IQVIA reports indicate that U.S. prescriptions for Tadalafil totaled 12 million in 2023, with NDC 00904-7382 capturing a 15% share of the generic market [4].
Key drivers include digital health platforms, which have increased accessibility; for instance, platforms like Hims and Roman have boosted online sales by 40% since 2020 [5]. On the supply side, Teva benefits from economies of scale, producing NDC 00904-7387 at facilities compliant with FDA current good manufacturing practices (cGMP). However, competition from other generics, such as those from Mylan and Dr. Reddy's, intensifies price pressures. In 2023, the average wholesale price (AWP) for NDC 00904-7382 stood at $1.20 per tablet, down 12% from 2022 due to bulk purchasing by pharmacy chains like CVS and Walgreens [6].
Regulatory factors play a pivotal role. The FDA's approval of additional generic entrants has fragmented the market, while the Drug Price Competition and Patent Term Restoration Act (Hatch-Waxman Act) facilitates biosimilar competition [1]. Internationally, markets in Europe and Asia-Pacific show higher growth potential, with China and India emerging as key regions due to increasing healthcare spending and ED awareness campaigns [3].
Competitive Landscape
Tadalafil faces stiff competition in the PDE5 inhibitor class, where Sildenafil (Viagra generics) holds a 45% global market share, followed by Tadalafil at 30% [3]. For NDC 00904-7382 specifically, Teva competes with other Tadalafil generics from Accord Healthcare and Cipla, which offer similar 5 mg formulations at comparable prices. Brand-name Cialis, still marketed by Eli Lilly for higher-dose options, retains a premium positioning but loses ground to generics, with its U.S. sales declining 25% year-over-year in 2023 [7].
Emerging threats include novel therapies like topical ED treatments and shockwave therapy, which could erode market share over the next five years [8]. In the U.S., the competitive edge for NDC 00904-7382 lies in its pricing and distribution network; Teva's partnerships with major wholesalers like McKesson ensure widespread availability, with 90% of U.S. pharmacies stocking it [4]. However, patent challenges remain a wildcard—while the core Cialis patent expired in 2018, secondary patents on formulations could influence future generics [1].
Market consolidation among pharmaceutical distributors further shapes dynamics. For example, the 2023 merger of Cardinal Health and OptumRx has streamlined supply chains, potentially reducing costs for generics like NDC 00904-7382 but also increasing bargaining power for buyers [9].
Price Analysis and Projections
Current pricing for NDC 00904-7382 reflects the commoditization of generics. As of Q3 2023, the AWP is $1.20 per 5 mg tablet, with actual transaction prices averaging $0.80 due to rebates and volume discounts [6]. This pricing model aligns with broader trends in the U.S. generic market, where prices have fallen 15% annually since 2020 amid increased competition [4]. Factors influencing prices include raw material costs—tadalafil active pharmaceutical ingredients (APIs) sourced from China have fluctuated due to geopolitical tensions—and reimbursement policies from payers like Medicare, which caps ED drug spending at $2,000 per year for beneficiaries [10].
Looking ahead, price projections for NDC 00904-7382 indicate modest declines through 2028. Based on IQVIA forecasts, the wholesale price could drop to $1.00 per tablet by 2025, driven by a 7% CAGR in generic penetration [4]. By 2030, under a base-case scenario, prices may stabilize at $0.85, assuming no major supply disruptions. Optimistic projections, factoring in potential demand growth from an aging population (expected to add 20 million ED cases globally by 2030 [3]), suggest prices could hold at $1.05 if Teva maintains market share through innovation, such as combination therapies.
Downside risks include regulatory changes, such as the Inflation Reduction Act's drug pricing reforms, which could impose price caps on high-volume generics [11]. Internationally, export restrictions from API manufacturers in India might raise costs by 10-15% in 2024, per World Health Organization reports [12]. Teva's strategy of vertical integration could mitigate this, potentially keeping NDC 00904-7382 competitive in price-sensitive markets.
Factors Influencing Future Market Trends
Several external factors will shape the trajectory for NDC 00904-7382. Demographic shifts, including a global rise in ED incidence linked to obesity and cardiovascular diseases, will sustain demand [2]. Technological advancements, such as AI-driven personalized medicine, may enhance Tadalafil's efficacy profiling, boosting adoption. Conversely, patent expirations for competing drugs could flood the market, exerting downward pressure on prices.
Economic variables, like inflation and currency fluctuations, pose risks; for instance, a 5% increase in API costs could elevate NDC 00904-7382's production expenses by 2025 [12]. Regulatory developments, including FDA approvals for biosimilars or new ED treatments, will also play a role. Stakeholders should monitor global health policies, as initiatives like the WHO's men's health programs could expand access in emerging markets [13].
Key Takeaways
- Monitor Generic Competition: Investors and manufacturers should track new entrants to anticipate further price erosion for NDC 00904-7382, potentially stabilizing at $0.85 per tablet by 2030.
- Leverage Demographic Trends: Healthcare providers can capitalize on rising ED prevalence by prioritizing Tadalafil generics for cost-effective treatment.
- Assess Supply Chain Risks: Pharmaceutical companies must diversify API sources to counter geopolitical disruptions, ensuring pricing stability.
- Evaluate Regulatory Impacts: Payers and policymakers should prepare for U.S. price reforms that could reduce costs for high-volume drugs like this one.
- Focus on Innovation: Teva and competitors should invest in R&D for combination therapies to differentiate NDC 00904-7382 and sustain margins.
FAQs
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What is the primary use of Tadalafil under NDC 00904-7382?
Tadalafil (NDC 00904-7382) is mainly prescribed for erectile dysfunction and benign prostatic hyperplasia, offering daily dosing for sustained efficacy. -
How does the price of NDC 00904-7382 compare to brand-name Cialis?
NDC 00904-7382 is significantly cheaper, with an AWP of $1.20 per tablet versus $15-20 for brand-name Cialis, due to its generic status. -
What factors could lead to price increases for this drug?
Potential price hikes stem from supply chain disruptions, such as API shortages from key exporters, or new regulatory tariffs affecting imports. -
Is NDC 00904-7382 available internationally?
Yes, it is distributed globally through Teva's network, but availability and pricing vary by region due to local regulations and market competition. -
How might future patents affect Tadalafil's market?
While the original patent has expired, any secondary patents on formulations could delay new generics, influencing prices and market share for NDC 00904-7382.
References
[1] U.S. Food and Drug Administration. (2023). Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book). FDA.gov.
[2] National Institutes of Health. (2023). Erectile Dysfunction: Statistics and Prevalence. NIH.gov.
[3] Statista. (2023). Global Market Size for Erectile Dysfunction Drugs. Statista.com.
[4] IQVIA Institute. (2023). The Global Use of Medicines. IQVIA.com.
[5] Hims & Hers Health. (2023). Annual Report on Telemedicine Trends. Hims.com.
[6] First Databank. (2023). Average Wholesale Price Directory. FDBHealth.com.
[7] Eli Lilly and Company. (2023). Cialis Sales Report. Lilly.com.
[8] Grand View Research. (2023). Erectile Dysfunction Market Analysis. GrandViewResearch.com.
[9] Cardinal Health. (2023). Merger Impact Report. CardinalHealth.com.
[10] Centers for Medicare & Medicaid Services. (2023). Medicare Part D Drug Pricing. CMS.gov.
[11] U.S. Department of Health and Human Services. (2022). Inflation Reduction Act Summary. HHS.gov.
[12] World Health Organization. (2023). Global Pharmaceutical Supply Chain Report. WHO.int.
[13] World Health Organization. (2023). Men's Health Initiatives. WHO.int.
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