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Our tamper-evident PP blister packaging is a regulatory-compliant, custom-engineered solution designed to guarantee the integrity and safety of pharmaceutical products throughout their full lifecycle, from manufacturing to end-user consumption. As a leading provider of custom tamper-proof blister packaging for pharmaceutical products, Yuxuan Plastic Packaging utilizes pharmaceutical-grade polypropylene (PP) resin and precision thermoforming technology to create robust, tamper-evident packaging that prevents unauthorized access, counterfeiting, and contamination. Tailored to the strict requirements of pharmaceutical enterprises and commercial clients, our packaging delivers uncompromising product protection, full regulatory compliance, and clear visual tamper evidence to build trust with regulators and end-users.
Our tamper-evident PP blister packaging features a proprietary one-time-use seal structure that leaves highly visible, irreversible signs of tampering if the package is opened or altered. This includes frangible seals, tear-away lidding, and cavity-specific tamper indicators, ensuring unauthorized access is immediately detectable by manufacturers, distributors, and end-users.
Crafted from premium pharmaceutical grade polypropylene blister packaging resin, our products are non-toxic, non-leaching, and fully compatible with a wide range of pharmaceutical formulations, including tablets, capsules, powders, and liquid doses. The material exhibits exceptional chemical inertness, preventing any interaction that could compromise product efficacy or safety.
Our precision thermoforming process delivers consistent wall thickness and uniform seal surfaces, ensuring a hermetic seal that blocks moisture, oxygen, and microbial contamination. This exceptional barrier performance extends product shelf life, maintains drug potency, and meets strict pharmaceutical storage requirements.
We offer integrated child-resistant tamper-evident blister packs that meet global child safety standards, while maintaining accessibility for elderly and disabled users. Our custom designs balance safety and usability, with adjustable resistance levels to match your product’s risk profile and regulatory requirements.
All our pharmaceutical blister packaging is manufactured in GMP-compliant cleanroom facilities, adhering to US FDA 21 CFR, EU GMP, USP Class VI, and EP 3.1.3 standards.
Parameter | Specification Details |
Base Material | Pharmaceutical-Grade Polypropylene (PP) Homopolymer/Copolymer |
Material Thickness Range | 0.15 mm – 1.5 mm |
Seal Strength | ≥25 N/15mm (consistent hermetic seal performance) |
Operating Temperature Range | -10℃ × 130℃ (autoclavable options available) |
Water Vapor Transmission Rate (WVTR) | ≤0.5 g/m²·24h (38℃, 90% RH) |
Oxygen Transmission Rate (OTR) | ≤1.2 cc/m²·24h·atm (23℃, 0% RH) |
Dimensional Tolerance | ±0.03 mm for precision cavity forming |
Tamper-Evident Types | Frangible seal, tear-away lidding, cavity break-off indicators, perforated edge designs |
Compliance Standards | US FDA 21 CFR Part 117, EU GMP, USP Class VI, EP 3.1.3, ISO 15378 |
Our sterile blister packaging for medicine serves a wide range of pharmaceutical and healthcare sectors, with tailored solutions for prescription & OTC pharmaceutical manufacturing, nutraceutical & dietary supplement production, vaccine & biologic product handling, medical device & diagnostic kit packaging, and veterinary pharmaceutical production. Each design is optimized to meet the unique regulatory and performance needs of the target sector.
As a trusted packaging partner for pharmaceutical enterprises and commercial clients worldwide, Yuxuan combines specialized pharmaceutical packaging expertise, GMP-compliant cleanroom production, and unwavering regulatory compliance to deliver exceptional value. Our in-house R&D team provides end-to-end support from concept and prototype development to full-scale commercial production, ensuring every solution meets your product’s unique needs and global regulatory requirements. We implement a fully traceable quality management system, with rigorous testing at every production stage to guarantee consistent material safety, seal integrity, and tamper-evident performance. With flexible production capacity, fast regulatory-aligned lead times, and global shipping capabilities, we support both clinical trial batches and high-volume ongoing commercial manufacturing.
Yes. All our pharmaceutical packaging is produced in Class 100,000 cleanroom facilities fully compliant with GMP standards, with strict environmental controls and full batch traceability for every production run.
Absolutely. Our engineering team develops fully integrated child-resistant tamper-evident blister packs that meet both global tamper-evident regulations and child safety standards, with custom designs balanced for intended user accessibility.
Yes. All our pharmaceutical-grade PP materials comply with US FDA 21 CFR Part 117, EP 3.1.3, and USP Class VI standards, with full material safety data sheets and compliance documentation available for all commercial clients.
We offer flexible MOQs to accommodate clinical trial batches and full commercial production, with custom solutions available for orders starting from 10,000 units, depending on design complexity and size.
