Desiccant Bags for API

Desiccant Bags for API
Product Description

Envelope
Tyvek® (spunbonded polyethylene): 100% dust-free, suitable for direct contact with pharmaceutical and food products. Also available in DIN Type B non-woven (dust release ≤ 1 mg/unit) and FSC®-certified paper coated with compostable bioplastic (100% plastic-free, fully dust-proof).
Desiccant
Silica gel, activated clay, molecular sieve (3 Å or 4 Å) or tailored blends. All desiccants are non-toxic, non-corrosive, chemically inert and non-deliquescent. Free from DMF, biocides, fungicides, GMOs, PFAS, phthalates and SVHC under REACH.
Quality and compliance
Manufactured under ISO 9001 (certified since 1999). Produced in conformity with DIN 55473 (DIN CERTCO 5B002, since 1998) and MIL D-3464 Type I and Type II. Full batch traceability of raw materials and all components, including packaging. DMF absence verified by laboratory analysis per European Commission Decision C (2009) 1723; declaration of conformity available on request. 100% Made in Italy.

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Levosil Spa

  • Country/Region:
    Italy
  • Founded:
    1964
  • On CPHI since:
    2018
  • Certificates:
    3
  • Employees:
    25 - 49
Company types
Packaging supplier/manufacturer
Primary activities
Packaging materials
View company profile
Categories
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Specifications
  • Details
    Levosil desiccant bags protect moisture-sensitive pharmaceutical products throughout manufacturing, storage and distribution, preventing degradation, caking and loss of potency.

    Active Pharmaceutical Ingredients (APIs)
    Bulk API drums, fibre drums and lined containers. Desiccant bags maintain low relative humidity inside the packaging, protecting hygroscopic substances from moisture uptake during storage and transport. Available in weights from a few grams to several hundred grams, sized to the container volume and API sensitivity.

    Finished dosage forms
    Secondary and tertiary packaging of tablets, capsules, powders and granules in cartons, shippers and palletised loads, where blister or bottle-level protection alone is not sufficient.

    Medical devices and IVD
    Packaging of surgical instruments, implantable devices, diagnostic kits and reagents where corrosion,...

  • Selling Points
    Packaging; WHY LEVOSIL

    Micro Bags are manufactured under ISO 15378 (GMP for primary packaging materials) and supported by a Type III Drug Master File, enabling fast supplier qualification and direct reference in regulatory submissions.

    All production takes place at a single facility in Turin, Italy, with full batch traceability of every component. Production areas and finished products undergo annual microbiological testing, verifying the absence of mould spores and contaminants.

    The Tyvek® envelope guarantees zero dust release, suitable for clean room use and direct product contact. Also available in FSC®-certified compostable paper for plastic-free packaging targets.

    All desiccants are free from DMF, PFAS, biocides, phthalates and SVHC under REACH.

    From 0.25 g Micro Bags for blisters to large-format bags for API drums — one supplier, one quality system, one audit.

  • Supplied from
    Italy
  • Measured In
    piece
More specifications Fewer specifications

Levosil Spa

  • Country/Region:
    Italy
  • Founded:
    1964
  • On CPHI since:
    2018
  • Certificates:
    3
  • Employees:
    25 - 49
Company types
Packaging supplier/manufacturer
Primary activities
Packaging materials
View company profile

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