LDPE bags are produced from low-density polyethylene resin, offering excellent puncture resistance and sealability for secure packaging.
They provide chemical inertness, non-toxicity, and compliance with global standards like USFDA, ensuring product safety.
Yes, LDPE is recyclable, supporting sustainable practices in the pharmaceutical industry.
When stored properly, empty LDPE bags maintain integrity for years without degradation.
They withstand temperatures up to 95°C, suitable for most pharma storage conditions.
Fill in a controlled cleanroom environment using automated or manual funnels to prevent contamination.
Use impulse heat sealers at 120-150°C for airtight closures that block moisture ingress.
Keep in a cool, dry place away from sunlight and chemicals to preserve material properties.
No, single-use only for pharma to avoid cross-contamination risks.
Check for tears, pinholes, or weak seals using visual and leak tests before filling.
From 10x15 cm pouches to 100x120 cm liners, fully customizable.
Yes, custom printing for branding, batch numbers, and compliance info.
USFDA, EU 10/2011, and GMP compliant for global pharma use.
Free samples for qualified buyers to test compatibility.
Starts at 10,000 units, scalable for bulk needs.
USFDA 21 CFR, EU guidelines, and ISO 15378 for primary packaging materials.
It prevents hydrolysis and degradation in hygroscopic drugs, ensuring efficacy.
Recyclable LDPE reduces plastic waste compared to multi-layer alternatives.
Shift to high-barrier, eco-friendly films and smart packaging with indicators.
CDSCO mandates GMP and stability testing for all primary packaging like LDPE.
These bags use virgin LDPE resin with densities around 0.92-0.933 g/cm³, offering melt indices of 0.7-2.0 g/10 min, tensile strength >1500 PSI, and tear strength up to 450 lbs/inch for superior durability.
Antistatic agents and flame retardants reduce surface resistivity, preventing electrostatic discharge that could damage sensitive APIs or electronics during handling and gamma sterilization up to 50 kGy.
In-house FT-IR, DSC, tensile, seal, and burst strength tests confirm low leachables/extractables, endotoxin levels, and cleanroom production under GMP, meeting USP Class VI and EU 10/2011 standards.
Typically 12µm PET (outer), 9-30µm Aluminum Foil (barrier), and 75µm LDPE (inner contact layer), ensuring peel strength >150 g/15mm between layers for durability.
MVTR <0.5 g/m²/day, OTR near zero, and full block of UV/light/oxygen, ideal for long-term stability of hygroscopic powders in humid climates.
FT-IR for material ID, tensile strength >3000 PSI (ASTM D882), burst/seal strength >10-18 lbs/inch, and extractables/leachables per USP <661> with no heavy metals.
Made from virgin LDPE resin (density 0.92 g/cm³), with tensile strength >2200 PSI (ASTM D882), seal strength >30 N/25mm, and puncture resistance >6 lbs, matching production batches.
Gamma-irradiated up to 25-50 kGy, USP Class VI compliant, low leachables (<3000 ng/cm³ outgassing), and tested via FT-IR/DSC for material purity before dispatch.
Available in sizes 10x15 cm to 50x80 cm, antistatic or plain, with heat-seal or zipper options; minimum 5-10 pieces per type for compatibility trials.
Tensile strength 2200-3000 PSI (ASTM D882), elongation >500%, and puncture resistance >6 lbs support handling heavy bulk drugs without tears during transit.
Moisture vapor transmission rate (MVTR) <1 g/m²/day, chemical inertness to acids/bases, and antistatic additives prevent hydrolysis, static damage, and contamination in humid zones.
Gamma sterilizable to 25-50 kGy, USP <661> compliant for extractables, and cleanroom Class 100 production with FT-IR/DSC testing for purity in API/excipient handling.
75-150 µm gauge LDPE with heat-seal strength >10-18 lbs/inch (ASTM D882) prevents micro-leaks, maintaining <2% RH inside for 12+ months shelf life.
MVTR <0.5 g/m²/day at 38°C/90%RH, density 0.92 g/cm³, and UV stabilizers block hydrolysis and photodegradation, compliant with USP <671> container testing.
Produced in ISO Class 100, gamma sterilizable to 25 kGy, low particulates (<1000 particles/ft²), and extractables <5 ppm per EU 10/2011 for direct capsule contact.
Density 0.92 g/cm³ (ASTM D1505), tensile strength >2200 psi MD/TD (ASTM D882), elongation >300-350%, and 4 mil (100 µm) thickness for durability without shedding.
Low outgassing <3000 ng/cm³, MVTR 0.15 g/100in²/24hrs (ASTM F1249), puncture resistance >6 lbs (MIL-STD-3010), and double-bagged packaging minimize ions, NVR, and particulates.
Heat-sealable at 250-375°F with >30 N/25mm strength (ASTM F88), gamma-compatible up to 50 kGy, and antistatic surface resistivity for ESD-safe handling in pharma cleanrooms.
Density 0.92-0.933 g/cm³, tensile strength >2500 PSI (ASTM D882), dart impact >300 g, and thicknesses 150-300 µm withstand 25-50 kg loads without rupture.
MVTR <0.8 g/m²/day at 38°C/90%RH, OTR <50 cc/m²/day, and inert to pH 2-12 chemicals prevent degradation, oxidation, and microbial growth for 24+ months.
USP <661>/<671> for extractables/particulates, gamma sterilization to 40 kGy, and seal integrity >20 lbs/inch (ASTM F88) under GMP cleanroom production.
Thickness 75-150 µm, tensile strength >2200 psi MD/TD (ASTM D882), and elongation >500% prevent cracking or dust generation during bulk handling and vibration transit.
MVTR <0.5 g/m²/day at 40°C/90%RH (ASTM F1249), combined with airtight heat seals >30 N/25mm, ensure <20% RH inside, preventing softening or capping over 24 months.
USP Class VI, low extractables <10 ppm (USP <661>), gamma sterilizable to 25-40 kGy, and cleanroom Class 100 production with particulates <100/ft² for direct product contact.
Yes, LDPE bags are non-toxic, chemically resistant, and compliant with FDA and EU regulations, making them safe for pharmaceutical use.<
Yes, LDPE bags can meet GMP standards when manufactured from pharma-grade resins under controlled cleanroom conditions.
Yes, LDPE bags can be sterilized using methods such as gamma irradiation or ethylene oxide, ensuring they remain suitable for pharmaceutical packaging.
Pharmaceutical LDPE (Low-Density Polyethylene) bags are primarily used for packaging, storing, and transporting pharmaceutical products, ensuring product safety and compliance with industry standards.
LDPE bags offer flexibility, durability, moisture resistance, and chemical stability, making them ideal for pharmaceutical packaging.
Pharmaceutical LDPE bags are available in a wide range of sizes and thicknesses, typically from 30 microns to 200 microns, depending on product requirements.
Yes, LDPE bags can be customized in terms of size, thickness, printing, and sealing options to meet specific pharmaceutical needs.
LDPE bags should be stored in a clean, dry environment away from direct sunlight and extreme temperatures to maintain integrity.
