IndiaMart
FIEO
In the competitive world of pharmaceuticals, third-party manufacturing has become a strategic tool for businesses looking to streamline production, reduce costs, and ensure consistent quality. At our state-of-the-art manufacturing facility, we specialize in the third-party manufacturing of Cenforce LD (Low Dose) tablets—a trusted medication for erectile dysfunction (ED) management. Our dedication to innovation, compliance, and customer satisfaction makes us the preferred partner for companies seeking to expand their portfolio with reliable ED medications.
Why Choose Our Third-Party Manufacturing Services for Cenforce LD?
1. Expertise in Sildenafil Citrate Formulations
Cenforce LD contains Sildenafil Citrate, the gold-standard PDE5 inhibitor for treating erectile dysfunction. Our facility employs experienced pharmaceutical scientists and formulation experts who have a deep understanding of sildenafil’s pharmacokinetics and stability requirements. We ensure precise low-dose formulation, which is ideal for patients needing milder interventions or those who are more sensitive to standard doses.
2. WHO-GMP & ISO Certified Facility
We manufacture Cenforce LD tablets in a facility accredited with WHO-GMP and ISO 9001 certifications. These globally recognized standards guarantee that every stage—from sourcing active pharmaceutical ingredients (APIs) to packaging—is done under stringent quality controls, ensuring product safety, efficacy, and consistency.
3. Stringent Quality Control & Assurance
Our in-house Quality Control (QC) and Quality Assurance (QA) teams implement rigorous testing protocols at every stage of production. We perform:
- Identity, purity, and potency tests on raw materials.
- In-process controls during tablet compression, granulation, and coating.
- Finished product testing for uniformity, dissolution, and stability.
Every batch of Cenforce LD is accompanied by a Certificate of Analysis (COA), ensuring full transparency and compliance with pharmacopeial standards.
4. Flexible Batch Sizes & Customization
Whether you’re a startup exploring niche markets or an established pharmaceutical company needing high-volume production, we offer flexibility in batch sizes—from pilot batches for market testing to commercial-scale production. We also provide:
- Customizable tablet strengths (e.g., 25 mg, 50 mg).
- Different tablet shapes, colors, and film coatings.
- Packaging options tailored to your brand identity.
5. Advanced Manufacturing Technology
Our facility houses advanced high-speed tablet compression machines, automated coating systems, and blister packaging lines. This technological edge ensures consistent tablet quality with precise weight, hardness, and disintegration profiles for Cenforce LD.
6. End-to-End Third-Party Manufacturing Solutions
From formulation development to final packaging and logistics support, our comprehensive third-party manufacturing service covers every aspect. This allows you to focus on marketing, distribution, and sales, while we take care of the technical, regulatory, and production details.
7. Regulatory Compliance & Documentation Support
Understanding the complexities of pharmaceutical regulations across global markets, we assist our clients in preparing essential documents, including:
- Drug Master Files (DMFs)
- Stability data reports
- Good Manufacturing Practice (GMP) certificates
- Dossiers for domestic and international registrations
This helps accelerate market approvals and ensures compliance with agencies like the US FDA, UK MHRA, EU EMA, and others.
Our Manufacturing Process for Cenforce LD Tablets
a) API Procurement
We procure high-purity Sildenafil Citrate from certified API suppliers who meet pharmacopeial specifications (USP/BP/EP). Each API batch undergoes verification before release into production.
b) Granulation
The API and excipients are blended and granulated under controlled humidity and temperature conditions to achieve uniform distribution and flow properties.
c) Compression
Granules are compressed into tablets using rotary tablet presses equipped with online weight monitoring, ensuring uniform low-dose content critical for Cenforce LD’s therapeutic effect.
d) Coating
Tablets are film-coated using automated coating pans with precise control of spray rate and temperature, providing a professional finish and improved patient acceptability.
e) Packaging
We offer a wide range of packaging options, including alu-alu, blister packs, and bottles, all labeled in compliance with your branding and local regulations.
f) Warehousing & Dispatch
Finished products are stored in climate-controlled warehouses and dispatched using validated logistics partners, ensuring timely delivery without compromising product stability.
Value-Added Services
To further support our partners, we offer:
- Graphic design & printing for boxes, strips, and leaflets.
- Brand registration assistance in India and export markets.
- Pharmacovigilance support to help you manage post-marketing surveillance requirements.
- Custom labeling & serialization solutions to comply with track-and-trace regulations worldwide.
Benefits of Partnering with Us for Cenforce LD Manufacturing
Cost Efficiency: Leverage economies of scale with our large-capacity facility to reduce your production costs.
Speed to Market: Our streamlined processes ensure reduced lead times, helping you launch products faster.
Confidentiality: We respect the privacy of your formulations, brand information, and market strategies under strict non-disclosure agreements.
Sustainability Practices: Our eco-friendly manufacturing systems minimize waste, energy consumption, and carbon footprint, aligning with global sustainability goals.
Frequently Asked Questions (FAQs)
Q1: Can you manufacture Cenforce LD under my brand name?
Yes, we offer complete private labeling services so you can market Cenforce LD under your own brand.
Q2: Do you support international exports?
Absolutely. We comply with all international shipping regulations and offer end-to-end export documentation services.
Q3: What is the minimum order quantity (MOQ)?
Our MOQs are flexible, depending on your market needs, with options starting from small commercial batches.
Q4: How do you ensure patient safety?
We strictly adhere to pharmacopeial standards, perform stability testing, and maintain full traceability of raw materials and finished goods.
