IndiaMart
FIEO
BluepillExpress stands as a trusted name in the global pharmaceutical industry, offering third-party manufacturing services for a wide array of pharmaceutical formulations. As a fully certified and internationally accredited manufacturer and exporter, we cater to clients across more than 140 countries. Our commitment to quality, affordability, compliance, and timely delivery has made us a reliable partner for healthcare brands and pharmaceutical distributors worldwide.
One of our prominent offerings in the nonsteroidal anti-inflammatory drug (NSAID) category is Slow Diclofenac. BluepillExpress provides third-party manufacturing services for Slow Diclofenac tablets and capsules, ensuring consistent efficacy, safety, and superior shelf stability.
Introduction to Slow Diclofenac
Slow Diclofenac, also known as Diclofenac Sodium Sustained-Release (SR) or Extended-Release Diclofenac, is a modified-release formulation of Diclofenac designed to deliver the active ingredient gradually over a longer period. This ensures prolonged pain relief and reduced dosing frequency.
Therapeutic Class:
Nonsteroidal Anti-inflammatory Drug (NSAID)
Available Dosages at BluepillExpress:
- Slow Diclofenac 75 mg
- Slow Diclofenac 100 mg
These dosage forms can be manufactured as:
- Sustained-Release Tablets
- Extended-Release Capsules
Pharmacological Profile
Mechanism of Action
Slow Diclofenac works by inhibiting the cyclooxygenase (COX) enzymes—COX-1 and COX-2—thus reducing the synthesis of prostaglandins responsible for inflammation, pain, and fever. The sustained-release nature of the formulation allows for a steady release of the drug over 12 to 24 hours, making it suitable for chronic pain management and long-term treatment.
Indications
Our third-party manufactured Slow Diclofenac is indicated for the following conditions:
- Rheumatoid Arthritis
- Osteoarthritis
- Ankylosing Spondylitis
- Chronic back pain
- Post-operative pain
- Musculoskeletal injuries
- Gout
- Dental pain
- Dysmenorrhea (menstrual pain)
Advantages of Partnering with BluepillExpress for Slow Diclofenac Manufacturing
1. WHO-GMP Certified Facilities
All BluepillExpress manufacturing units comply with WHO-GMP, ISO, and Schedule M guidelines. Our facilities maintain cleanroom environments, advanced quality control systems, and high-standard practices, ensuring global compliance.
2. Flexible Batch Sizes
Whether you’re a startup brand or an established pharmaceutical marketer, we offer low to high batch-size flexibility, giving you cost-effective scalability without compromising quality.
3. Comprehensive Regulatory Support
We provide full documentation support including:
- Certificate of Analysis (CoA)
- Batch Manufacturing Record (BMR)
- Certificate of Pharmaceutical Product (COPP)
- Product dossiers for international registrations
- MSDS and Stability Data
- Export Documentation (if applicable)
4. Custom Branding and Private Labelling
We offer customized branding solutions, enabling you to launch your label in domestic or international markets seamlessly. From logo design to packaging material procurement, BluepillExpress assists you at every step.
5. Global Export Capabilities
BluepillExpress exports Slow Diclofenac formulations to various regions including:
- Latin America
- Africa
- Southeast Asia
- CIS nations
- Middle East
- Europe (as per registration)
- Oceania
Formulation & Manufacturing Excellence
Core Formulation Benefits
Our Slow Diclofenac formulations are engineered with:
- Modified-release excipients for time-controlled drug delivery
- Enteric coating (optional) to minimize gastrointestinal side effects
- Stabilizers to ensure consistent potency throughout shelf life
- Patient-centric design (easy-to-swallow, high bioavailability)
Manufacturing Process Flow:
- Pre-formulation & Raw Material Analysis
- API and excipient testing
- Compliance with pharmacopeial standards (USP/BP/EP)
- Granulation
- Wet or dry granulation based on formulation requirement
- Compression or Encapsulation
- Accurate dosing with state-of-the-art tablet presses or capsule fillers
- Coating & Polishing
- Sustained-release coatings using modern fluid-bed technology
- Quality Control Checks
- Uniformity of weight
- Dissolution profiling
- Assay of active content
- Microbial limit tests
- Packaging
- Blister packs, strip packs, and bottle packs available
- High-barrier packaging options for enhanced shelf life
Packaging Options
We provide customized packaging options as per client and market requirements:
- Alu-Alu Blister Packs
- PVC Blister Packs
- Aluminum Strip Packs
- HDPE Bottle Packs
- Sachets (on request)
All packaging options come with multicolor printing and serialization, compliant with track & trace regulations where applicable.
Why Choose BluepillExpress for Your Slow Diclofenac Manufacturing Needs?
1. Unmatched Industry Experience
With years of pharmaceutical expertise, BluepillExpress has developed strong technical knowledge and formulation capabilities. We understand the nuances of NSAID production, including stability challenges, patient compliance, and regulatory expectations.
2. Dedicated Project Management
Each client is assigned a dedicated account manager and regulatory associate who oversee your project from product development to final dispatch.
3. Timely Delivery
Our supply chain infrastructure ensures timely procurement of raw materials and streamlined production schedules, ensuring faster turnaround times for domestic and export orders.
4. Stringent Quality Standards
All products go through in-process and finished product testing, with full traceability and documentation support. We follow ICH guidelines for stability and retain sample management.
Quality Control & Assurance
Our Quality Control (QC) and Quality Assurance (QA) teams work in tandem to monitor every stage of production. We utilize state-of-the-art equipment for:
- HPLC and UV Spectrophotometry
- Dissolution and disintegration tests
- Particle size analysis
- Microbial testing
The QA team performs regular internal audits and ensures compliance with:
- WHO-GMP
- GLP (Good Laboratory Practices)
- GDP (Good Documentation Practices)
Compliance & Certifications
BluepillExpress is equipped with the following certifications and accreditations:
- WHO-GMP
- ISO 9001:2015
- FSSAI (for nutraceutical add-ons)
- CE Certification (where required)
- DCGI and CDSCO approval for domestic supplies
- Registration assistance for country-specific regulations
Contract Manufacturing Process Overview
Here’s how you can get started with our third-party manufacturing services for Slow Diclofenac:
Step 1: Product Finalization
Select the dosage strength, form (tablet or capsule), and market-specific packaging requirements.
Step 2: Documentation & Quotation
Share necessary documents (drug license, GST, etc.). Receive a detailed quotation with timeline estimates.
Step 3: Product Approval & Sample Development
We formulate pilot batches and provide samples for your review and stability testing.
Step 4: Production & Quality Control
On receiving approval, full-scale manufacturing begins under stringent quality checks.
Step 5: Final Packing & Dispatch
Finished goods are packed, labeled, tested, and shipped as per your instructions.
Global Partnerships
We welcome partnerships with:
- Pharmaceutical marketing companies
- International distributors
- Government tenders
- Institutional buyers
- Online medicine retailers
- Telemedicine providers
Whether you’re launching a new product or expanding your current portfolio, BluepillExpress ensures smooth collaboration, full regulatory compliance, and high-quality output.
Conclusion
As chronic pain, osteoarthritis, and inflammation-related disorders continue to rise globally, the demand for reliable and effective sustained-release NSAIDs like Slow Diclofenac is growing rapidly. With BluepillExpress, you gain a third-party manufacturing partner committed to excellence in formulation, compliance, and delivery.
Our services go beyond production — we provide regulatory support, branding assistance, documentation aid, and most importantly, peace of mind.
