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Acetamoren Capsule

Acetamoren Capsule

Acetamoren Capsule (MK-777) is a synthetic, non-peptide small molecule highly valued in specialized research applications. As your manufacturing partner, we provide standardized, high-purity encapsulation services, ensuring consistency from milligram precision to large-scale production.

Product Introduction

Product Introduction

 

Acetamoren Capsule (MK-777) is a synthetic, non-peptide small molecule highly valued in specialized research applications. As your manufacturing partner, we provide standardized, high-purity encapsulation services, ensuring consistency from milligram precision to large-scale production.

 

Technical Manufacturing Specifications

 

Raw Material

Acetamoren Powder (MK777 Powder)

Capsule shell

Gelatin or Vegetarian Capsules

Capsule Size

0# / 1# / Custom Size

Label Material

PVC, Synthetic paper

Dosage

10 mg

MOQ

Flexible, starting from 500 units

Lead Time

Stock Formula:3 days

Custom Formula:7 days

Shelf Life

24 months under proper storage

Certificates

GMP, ISO, COA, Third-party Testing

 

Certification of Analysis:


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Compliance Note: Acetamoren is manufactured strictly for research and development purposes and professional ODM/OEM integration. We provide full technical documentation, including COA and MSDS, to support your product development and quality audits.

 

Customers' Satisfaction

 

We build long-term, trust-based relationships with our global partners. Our commitment to manufacturing excellence, consistent product quality, and reliable technical support has earned us the high satisfaction and continued partnership of top brands across the supplement and research sectors.

 

Customers' Good Comment

 

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OEM Service

 

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Manufacturing Capability

 

Our production infrastructure is designed to scale with your business, backed by industry-leading facilities:
Scalable Capacity: Our factory covers approx. 26,700 m² (40 mu), supporting a monthly capacity of up to 10 tons.
Versatile Infrastructure: We utilize high-performance reactors ranging from 200L to 5,000L, enabling precision production from milligram research scales to industrial tonnage.
Expert Team: Backed by a senior technical team with over 20 years of industry experience, we combine innovation, precision engineering, and strict quality control.
Dual-Market Compliance: Our GMP-compliant facilities support regulatory filing requirements in both China and the United States.

 

Quality Assurance & Certifications

 

We strictly adhere to established SOPs to ensure every batch meets international expectations.
Certifications: We hold FDA and HACCP credentials, alongside ISO 9001:2015 quality management certification.
Process Control: Rigorous quality supervision, in-process monitoring, and third-party analytical testing are standard for all production lots.
Traceability: From raw material sourcing to the finished product, our system guarantees total reliability and long-term stability.

 

One-Stop OEM/ODM Manufacturing Solutions

 

Xi'an Ruichi Biotech provides comprehensive services for brand owners, distributors, and healthcare companies worldwide. From product concept and formulation to manufacturing, private labeling, and customized packaging, we help you efficiently launch your products under your own brand.
Our Service Core:

  • Formula Optimization: Expert R&D support for complex supplement blends.
  • Custom Packaging: Tailored solutions to match your brand identity.
  • Global Logistics: Secure, professional shipping and customs support.

 

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FAQ

 

Q: What is the primary difference between your "Stock Formula" and "Custom Formula" services?

A: Stock formulas are pre-verified and ready for private labeling within 3 days. Custom formulas require a collaborative R&D phase, pilot testing, and stability trials, with a standard turnaround of 7 days.

Q: How do you handle third-party testing for specialized ingredients?

A: We conduct rigorous internal HPLC/MS analysis for every batch. We fully support and facilitate additional testing by independent, accredited laboratories upon request to ensure complete transparency for your quality control files.

Q: Can you assist with the regulatory documentation required for import?

A: Yes. We provide all necessary technical documentation, including COA, MSDS, and relevant ISO/GMP/FDA certification copies, to ensure smooth customs clearance in your target market.

Q: What is your policy regarding sample procurement for new B2B partners?

A: We offer a streamlined sample procurement process for verified B2B partners. Please contact our project manager with your business details to arrange samples for your internal quality validation.

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