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Sangesic Tablet & Patch

  • Sangesic Tablet & Patch 1
  • Sangesic Tablet & Patch 2
  • Sangesic Tablet & Patch 3
Product Description

Sangesic  Tablet :-1. Faster onset of action 
2. Better patient Compliance 
3. Long duration of action ( 6hrs tp 12 hrs.) 
4. Effective in moderate to severe pain management

Sangesic  Patch:- 
1. Well tolerated 
2. Continouse pain relief for 7 days
3. Improvement in physcial function
4. Signifacant reduction in pain intensity

Read more Show less

Rusan Pharma Ltd

  • IN
  • 2015
    On CPHI since
  • 2
    Certificates
  • 500 - 999
    Employees
Company types
Manufacturer/Innovator
Pharmaceutical company
Primary activities
API Producer
Pharmaceutical Company (innovator finished products)
View company profile
Categories
more categories Show less
Specifications
  • Details
    Sangesic  Tablet :-1. Faster onset of action 
    2. Better patient Compliance 
    3. Long duration of action ( 6hrs tp 12 hrs.) 
    4. Effective in moderate to severe pain management

    Sangesic  Patch:- 
    1. Well tolerated 
    2. Continouse pain relief for 7 days
    3. Improvement in physcial function
    4. Signifacant reduction in pain intensity
  • Model
    Buprenorphine Sublingual Tablet (0.2 mg)/ Buprenorphine Transdermal Patch (5 | 10 | 20 mcg/hr)
More specifications Fewer specifications

Rusan Pharma Ltd

  • IN
  • 2015
    On CPHI since
  • 2
    Certificates
  • 500 - 999
    Employees
Company types
Manufacturer/Innovator
Pharmaceutical company
Primary activities
API Producer
Pharmaceutical Company (innovator finished products)
View company profile

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Rusan Pharma Ltd resources (2)

  • Rusan Pharma’s API Plant in Ankleshwar (India) Receives USFDA GMP Approval

    News Rusan Pharma’s API Plant in Ankleshwar (India) Receives USFDA GMP Approval

    RUSAN PHARMA PRIVATE LIMITED, an Indian pharmaceutical company specializing in addiction treatment and pain management, announced that its Active Pharmaceutical Ingredient (API) facility in Ankleshwar, Gujarat, received Good Manufacturing Practice (GMP) approval from the USFDA on May 29, 2024, following a rigorous inspection. This approval marks a significant milestone, enabling Rusan to expand into the US API market, particularly for niche APIs like Eflornithine and Nalmefene, while planning to add more APIs to its portfolio. Rusan Pharma’s Managing Director, Dr. Kunal Saxena, emphasized the company’s commitment to quality and global expansion. The USFDA approval complements Rusan's existing GMP certifications from Health Canada, the EU, and Brazil’s ANVISA, and aligns with the company’s vision to be a leader in addiction treatment and pain management. 
    20 Sep 2024
  • Commercials APIs & APIs Under Development

    Technical Data Commercials APIs & APIs Under Development

    Commercials APIs  & APIs Under Development  

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