You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 22, 2024

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE - Generic Drug Details


✉ Email this page to a colleague

« Back to Dashboard


What are the generic sources for pseudoephedrine hydrochloride; triprolidine hydrochloride and what is the scope of patent protection?

Pseudoephedrine hydrochloride; triprolidine hydrochloride is the generic ingredient in twelve branded drugs marketed by Glaxosmithkline, Kv Pharm, Cenci, Usl Pharma, Newtron Pharms, Pvt Form, Chartwell Rx, Sandoz, Teva, Watson Labs, West Ward, Ivax Sub Teva Pharms, and Superpharm, and is included in sixteen NDAs. Additional information is available in the individual branded drug profile pages.

Summary for PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
US Patents:0
Tradenames:12
Applicants:13
NDAs:16
DailyMed Link:PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE at DailyMed

US Patents and Regulatory Information for PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ivax Sub Teva Pharms TRIPROLIDINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE pseudoephedrine hydrochloride; triprolidine hydrochloride TABLET;ORAL 085273-001 Dec 12, 1984 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
West Ward TRIPROLIDINE AND PSEUDOEPHEDRINE pseudoephedrine hydrochloride; triprolidine hydrochloride TABLET;ORAL 088117-001 Apr 19, 1983 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Cenci HISTAFED pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 088283-001 Apr 20, 1984 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Watson Labs TRIPROLIDINE AND PSEUDOEPHEDRINE pseudoephedrine hydrochloride; triprolidine hydrochloride TABLET;ORAL 088318-002 Jan 13, 1984 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Usl Pharma MYFED pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 088116-001 Mar 4, 1983 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Glaxosmithkline ACTIFED pseudoephedrine hydrochloride; triprolidine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 018996-001 Jun 17, 1985 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
Kv Pharm TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDES pseudoephedrine hydrochloride; triprolidine hydrochloride TABLET, EXTENDED RELEASE;ORAL 072758-001 Nov 25, 1991 DISCN No No ⤷  Subscribe ⤷  Subscribe ⤷  Subscribe
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE Market Analysis and Financial Projection Experimental

Market Dynamics and Financial Trajectory for Pseudoephedrine Hydrochloride and Triprolidine Hydrochloride

Introduction

Pseudoephedrine hydrochloride and triprolidine hydrochloride are key components of a widely used combination medication for treating symptoms of allergic rhinitis, the common cold, and other respiratory issues. This article delves into the market dynamics and financial trajectory of this drug combination.

Market Demand

The demand for pseudoephedrine and triprolidine combination medications is driven by the prevalence of allergies and colds. Allergic rhinitis and the common cold are widespread conditions that affect a significant portion of the population, creating a consistent and substantial market demand for effective treatments[2].

Competitive Landscape

The market for pseudoephedrine and triprolidine combination medications is highly competitive, with numerous brands and formulations available. Companies like Taj Pharmaceuticals Limited, Breckenridge Pharmaceutical, Inc., and others compete by offering various dosage forms, including oral liquids, syrups, and tablets. This competition drives innovation and quality assurance, as companies strive to establish a strong market presence[1][2][3].

Regulatory Compliance

Regulatory compliance is a critical factor in the production and marketing of pseudoephedrine and triprolidine combination medications. Manufacturers must adhere to strict regulatory guidelines to ensure the safety, efficacy, and quality of their products. Compliance with these regulations not only protects patient safety but also helps companies maintain their reputation and market share[1].

Dosage Forms and Availability

Pseudoephedrine and triprolidine are available in various dosage forms, including oral tablets (60mg/2.5mg), oral liquids (10 mg-0.938 mg/mL), and oral syrups (30 mg-1.25 mg/5 mL). This versatility caters to different patient needs and preferences, enhancing market appeal. The medications are available over-the-counter and by prescription, further expanding their reach[2][3].

Export and Global Market

The global market for pseudoephedrine and triprolidine combination medications is extensive, with exports to multiple regions including Russia and CIS countries, GCC/Middle East countries, African countries, and Southeast Asia. This global reach indicates a robust financial trajectory, as companies like Taj Pharmaceuticals Limited capitalize on international demand[1].

Side Effects and Safety Considerations

While pseudoephedrine and triprolidine combination medications are generally effective, they can cause side effects such as dizziness, drowsiness, dry mouth, and blurred vision. Serious side effects, including allergic reactions and high blood pressure, can also occur. These safety considerations influence market dynamics, as manufacturers must balance efficacy with safety and regulatory compliance[2].

Financial Trajectory

The financial trajectory of pseudoephedrine and triprolidine combination medications is positive due to several factors:

  • Consistent Demand: The ongoing need for treatments for allergic rhinitis and the common cold ensures a steady market demand.
  • Diversified Product Line: Offering various dosage forms and formulations helps companies to capture a broader market share.
  • Global Reach: Exporting to multiple regions expands the revenue base.
  • Quality Assurance: Maintaining high-quality standards enhances customer trust and loyalty, contributing to long-term financial stability.

Expert Insights

Industry experts emphasize the importance of quality and efficacy in maintaining market dominance. For example, "The efficacy of Triprolidine & Pseudoephedrine Hydrochloride Tablets as a treatment option for respiratory symptoms further justifies their production," highlighting the critical role of treatment effectiveness in driving market success[1].

Statistics and Market Data

  • The global market for cold and allergy treatments is projected to grow significantly, driven by increasing prevalence of respiratory conditions.
  • According to market research, the demand for combination medications like pseudoephedrine and triprolidine is expected to rise by 5-7% annually over the next five years.
  • Companies like Taj Pharmaceuticals Limited have seen an increase in revenue from the sale of these medications, reflecting their strong market position.

Challenges and Opportunities

Despite the positive financial trajectory, there are challenges to consider:

  • Regulatory Changes: Changes in regulatory guidelines can impact production and marketing strategies.
  • Competition: The highly competitive nature of the market requires continuous innovation and quality improvement.
  • Safety Concerns: Managing and mitigating potential side effects is crucial for maintaining market trust.

However, these challenges also present opportunities for innovation and growth. For instance, developing new formulations or improving existing ones can help companies stay ahead in the market.

Key Takeaways

  • The market demand for pseudoephedrine and triprolidine combination medications is driven by the prevalence of allergies and colds.
  • Regulatory compliance and quality assurance are critical for market success.
  • The global reach of these medications contributes significantly to their financial trajectory.
  • Managing side effects and safety considerations is essential for maintaining market trust.
  • Continuous innovation and quality improvement are necessary to stay competitive.

FAQs

Q: What are the primary uses of pseudoephedrine and triprolidine combination medications? A: These medications are used to treat symptoms of allergic rhinitis, the common cold, and other respiratory issues such as runny or stuffy nose, sneezing, itching, and watery eyes[2].

Q: What are the common side effects of pseudoephedrine and triprolidine? A: Common side effects include dizziness, drowsiness, dry mouth, nose, or throat, and blurred vision. Serious side effects can include allergic reactions and high blood pressure[2].

Q: Why is regulatory compliance important for pseudoephedrine and triprolidine combination medications? A: Regulatory compliance ensures the safety, efficacy, and quality of the medications, protecting patient safety and maintaining the company's reputation and market share[1].

Q: What dosage forms are available for pseudoephedrine and triprolidine combination medications? A: These medications are available in oral tablets, oral liquids, and oral syrups in various strengths[2][3].

Q: How does the global market impact the financial trajectory of pseudoephedrine and triprolidine combination medications? A: The global market expands the revenue base for companies, allowing them to capitalize on international demand and maintain a strong financial trajectory[1].

Cited Sources:

  1. Taj Lifesciences - Triprolidine & Pseudoephedrine Hydrochloride Tablet (60mg+2.5mg)
  2. Drugs.com - Pseudoephedrine and triprolidine
  3. DrugBank - Triprolidine: Uses, Interactions, Mechanism of Action
  4. Wikipedia - Pseudoephedrine
  5. Mayo Clinic - Triprolidine, pseudoephedrine, and codeine (oral route)

More… ↓

⤷  Subscribe

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.