AVA FORCE 200

AvaForce 200 is a high-dosage generic medication widely used to treat erectile dysfunction (ED) in men. Containing 200 mg of Sildenafil Citrate, it belongs to a class of drugs known as PDE5 inhibitors, which work by increasing blood flow to the penis during sexual stimulation. The demand for high-dosage ED medicines like AvaForce 200 has surged globally, especially in markets that favor strong, fast-acting solutions for male sexual health. For pharmaceutical companies looking to expand their product portfolio, third-party manufacturing of AvaForce 200 provides an efficient, low-risk opportunity.

This detailed guide explores how third-party manufacturing of AvaForce 200 works, its advantages, required certifications, packaging standards, regulatory considerations, and market potential.

Product Overview: AvaForce 200

Composition:

• Active Ingredient: Sildenafil Citrate
• Strength: 200 mg per tablet
• Form: Film-coated oral tablet
• Category: Erectile Dysfunction Treatment
• Pharmacological Action: PDE5 Inhibitor
• Shelf Life: 24–36 months depending on storage conditions
• Packaging: Blister packs, bottles, or customized as per client requirements

AvaForce 200 is generally recommended for men who do not respond adequately to lower dosages such as 50 mg or 100 mg. It offers a faster onset time and longer duration, enhancing sexual performance and patient satisfaction.

Benefits of Third-Party Manufacturing AvaForce 200

Outsourcing the production of AvaForce 200 to a third-party manufacturer offers several benefits for brand owners, wholesalers, and international pharmaceutical exporters:

1. Cost Efficiency

Manufacturing high-dosage medicines requires specialized equipment and skilled labor. Third-party manufacturers already have GMP-certified infrastructure in place, reducing your upfront capital investment.

2. Time-Saving

By outsourcing, companies can focus on branding, marketing, and distribution while the manufacturer handles the formulation, production, and packaging.

3. Scalability

With access to large-scale production capabilities, you can quickly ramp up or scale down manufacturing based on market demand.

4. Regulatory Support

Reputed third-party manufacturers help ensure compliance with international standards, including WHO-GMP, ISO, and DCGI approvals, enabling smooth export operations to regulated and semi-regulated markets.

5. Customization

From packaging design to tablet color and imprinting, manufacturers allow customization for private labeling under your brand.

Manufacturing Process for AvaForce 200

The production of AvaForce 200 involves the following key steps, ensuring safety, quality, and efficacy:

1. Sourcing of Raw Materials
   • Sildenafil Citrate API is sourced from certified suppliers.
   • Excipients like microcrystalline cellulose, magnesium stearate, and lactose are selected based on quality and compatibility.
2. Formulation Development
   • The 200 mg formulation is optimized for bioavailability and stability.
   • Tablets are coated to protect the drug from oxidation and moisture.
3. Manufacturing & Compression
   • The blend undergoes granulation, drying, and compression using high-speed tableting machines under controlled environmental conditions.
4. Quality Control (QC)
   • Each batch is tested for:
     • Active ingredient concentration
     • Disintegration and dissolution
     • Microbial contamination
     • Stability under different conditions
5. Packaging
   • AvaForce 200 is packed in tamper-proof blister strips or bottles.
   • Batch numbers, expiry dates, manufacturing license details, and dosage instructions are clearly printed.
6. Dispatch
   • Finished products are stored in temperature-controlled warehouses and dispatched with proper documentation for domestic or international shipping.

Key Certifications and Quality Standards

Third-party manufacturers of AvaForce 200 must comply with the following:

• WHO-GMP (World Health Organization – Good Manufacturing Practices)
• ISO 9001:2015 Certification
• DCGI (Drug Controller General of India) Approval
• FSSAI (For nutraceutical variations, if any)
• US FDA / EU-GMP (for regulated market supplies)

These certifications ensure that every batch of AvaForce 200 meets the highest pharmaceutical standards for efficacy, purity, and patient safety.

Packaging Options

To support your branding and market positioning, packaging for AvaForce 200 can be fully customized:

• Primary Packaging:
  • Blister packs (Alu-Alu or PVC)
  • Bottles (HDPE or glass)
  • Strip packs with foil printing
• Secondary Packaging:
  • Custom-printed cartons
  • QR code/Barcoding for inventory tracking
  • Multilingual labeling (as per export country requirement)

Eco-friendly packaging solutions can also be offered upon request, appealing to global buyers seeking sustainable products.

Target Export Markets

With demand growing rapidly across various regions, AvaForce 200 can be exported to:

• Latin America: Brazil, Mexico, Colombia
• Africa: Kenya, Nigeria, South Africa, Egypt
• Asia-Pacific: Philippines, Vietnam, Thailand, Indonesia
• CIS Countries: Russia, Kazakhstan, Ukraine
• Middle East: UAE, Saudi Arabia, Oman
• Unregulated/ semi-regulated markets with streamlined registration

For regulated markets like the EU or US, additional certifications may be required.

How to Partner with a Third-Party Manufacturer

To begin third-party manufacturing of AvaForce 200, follow these steps:

1. Select a certified manufacturer experienced in ED formulations.
2. Sign a legal agreement (LOI or MOU) outlining the scope, terms, and confidentiality clauses.
3. Submit your brand name, logo, and packaging preferences.
4. Approve samples before proceeding with commercial batch production.
5. Complete regulatory paperwork if exporting.
6. Receive delivery within the committed lead time (typically 25–40 days).

Why Choose Us for AvaForce 200 Third-Party Manufacturing?

As a trusted pharmaceutical manufacturer with over a decade of experience, we offer:

• State-of-the-art WHO-GMP production facilities
• Expert R&D team for formulation support
• Affordable MOQ (Minimum Order Quantity) for startups and exporters
• Rapid turnaround times and flexible supply options
• Multilingual customer support and logistics coordination
• Transparent pricing with no hidden costs

Final Thoughts

AvaForce 200 is a strategic product in the booming global ED medicine market. Partnering with a reliable third-party manufacturer enables you to capitalize on its demand without the burden of in-house production. With the right manufacturing partner, you can ensure consistent quality, fast delivery, and regulatory compliance—boosting your brand’s credibility and profit margins.

Whether you’re launching a new brand or expanding your product line, AvaForce 200 offers significant potential for growth in the pharma export business.