Product Description
Doripenem Injection 250 mg contains doripenem, a carbapenem antibiotic formulated as a sterile powder for intravenous administration. Manufactured using validated pharmaceutical processes, the medicine is developed to maintain sterility, formulation consistency, and product integrity throughout production.
Every vial is produced under controlled environmental conditions using internationally accepted manufacturing practices.
Mechanism of Action
Doripenem acts by inhibiting bacterial cell wall synthesis.
The medicine binds to penicillin-binding proteins (PBPs), preventing bacteria from forming a protective cell wall. As a result, susceptible bacteria lose structural integrity and are destroyed, helping control bacterial infections.
Product Overview
| Product Details | Information |
|---|---|
| Product Name | Doripenem Injection |
| Strength | 250 mg |
| Generic Name | Doripenem |
| Dosage Form | Sterile Powder for Injection |
| Route of Administration | Intravenous (IV) |
| Drug Category | Carbapenem Antibiotic |
| Packaging | Sterile Glass Vial |
| Country of Origin | India |
Key Features
- Doripenem sterile injectable formulation
- Carbapenem class antibiotic
- Sterile powder for injection
- WHO-GMP certified manufacturing
- High pharmaceutical purity
- Excellent formulation stability
- Reliable batch quality
- Advanced aseptic manufacturing
- Export-quality packaging
- International manufacturing standards
Recommended Dosage
Dosage should always be determined by a qualified healthcare professional.
Treatment depends on:
- Type of bacterial infection
- Severity of illness
- Patient age
- Body weight
- Kidney function
- Overall clinical assessment
The medicine should only be administered under professional medical supervision.
Possible Side Effects
Some patients may experience temporary side effects during treatment.
Possible reactions include:
- Headache
- Nausea
- Vomiting
- Diarrhea
- Injection site discomfort
- Skin rash
- Fever
- Dizziness
- Allergic reactions
- Temporary liver enzyme changes
Consult your healthcare provider if symptoms become severe or persistent.
Safety Information
- Prescription-only medicine.
- For intravenous administration by qualified healthcare professionals.
- Inform your doctor about previous antibiotic allergies.
- Complete the prescribed treatment course.
- Avoid using expired medicine.
- Keep out of reach of children.
- Follow all medical instructions carefully.
Storage Information
- Store below 25°C
- Protect from moisture
- Keep away from direct sunlight
- Store in original packaging
- Do not freeze
- Use before expiry date
Quality Assurance
At Ernest Oncology, every product is manufactured under stringent pharmaceutical quality systems to ensure safety and reliability.
Our Quality Standards
- WHO-GMP certified manufacturing facilities
- Sterility validation
- Batch-wise laboratory testing
- Raw material verification
- Stability testing
- Packaging inspection
- Product traceability
- Continuous quality monitoring
Documentation
The following documents are generally available:
- Certificate of Analysis (COA)
- Certificate of Origin (COO)
- Commercial Invoice
- Packing List
- Product Specification Sheet
- Certificate of Pharmaceutical Product (CPP)* (where applicable)
- Batch Manufacturing Record* (where applicable)
- Airway Bill / Bill of Lading
Washington Pharmaceutical Market Information
Washington continues to strengthen its healthcare infrastructure through modern hospitals, specialist treatment centres, emergency care units, and advanced medical research institutions. Injectable antibiotics remain essential for hospital-based patient management, creating demand for medicines manufactured according to internationally accepted pharmaceutical standards.
India has become one of the world's most respected pharmaceutical manufacturing destinations, supplying high-quality sterile injectables supported by advanced technology and rigorous quality systems.
Why Choose Indian Pharmaceutical Manufacturing
India is recognized globally for producing pharmaceutical products that combine quality, innovation, and manufacturing excellence.
Manufacturing Advantages
- WHO-GMP certified facilities
- Modern sterile injectable production
- International quality standards
- High pharmaceutical purity
- Reliable batch consistency
- Advanced quality control laboratories
- Export-quality packaging
- Scientific manufacturing expertise
- Continuous product improvement
- Trusted global pharmaceutical reputation