Polyvinyl chloride solid pharmaceutical tablets are a type of pharmaceutical packaging material that comes into direct contact with drugs. Quality control can be carried out in accordance with the YBB00212005-2015 "Polyvinyl chloride solid pharmaceutical tablets" standard.

The YBB00212005-2015 standard for solid medicinal hard sheets of polyvinyl chloride is applicable to hard sheets made mainly from polyvinyl chloride (PVC) resin. It is one of the more than 130 drug packaging material standards issued by the State Food and Drug Administration in 2015 for direct contact with drugs. The standard specifies the physical properties for blister packaging of solid drugs (tablets, capsules, etc.).

The testing indicators specified in YBB00212005-2015 "Solid Pharmaceutical Hard Tablets of Polyvinyl Chloride";

Take an appropriate amount of this product and visually inspect it in a bright natural light. The color should be uniform, and there should be no bumps, wrinkles, oil stains, foreign objects, perforations, or impurities. Within every 100 square meters, there shall be no more than 3 points with a diameter of 1.3mm or less, and no 1.3mm crystal points.

[Water vapor transmission rate] Take an appropriate amount of this product and measure the water vapor transmission rate according to YBBOOO92003-2015. The water vapor transmission rate should not exceed 2.5g (㎡). 24h）

Oxygen permeation rate: Take an appropriate amount of this product and measure it according to the gas permeation rate measurement method YBB00082003-2015. It should not exceed 30m3/

【 Tensile strength 】 This product is suitable for testing according to the tensile performance measurement method (YBBOO112003-2015), with a test speed (no load) of 100mm/min ± 10mm/min, and the sample is Type I. The average longitudinal and transverse tensile strength shall not be less than 44MPa.

【 Impact Resistance 】 Take an appropriate amount of this product and cut 5 pieces each of 150mm x 50mm in length and width. The sample shall be placed in an environment with a temperature of 23 ℃± 2 ℃ and a relative humidity of 50% ± 5% for more than 4 hours and tested under the specified conditions. Fix the sample on the drop ball impact testing machine with a span of 100mm. Select the steel ball and drop ball height according to 1, so that the steel ball falls freely to the center of the span, and there should be no more than 2 pieces of damage in both longitudinal and transverse directions.

【 Heating elongation rate 】 Take an appropriate amount of this product and measure it according to the heating elongation rate measurement method (YBB00292004-2015). The elongation rate should be within ± 6%.

【 Heat sealing strength 】 Take an appropriate amount of this product, cut 2 pieces of 1000mmx100mm samples, and stack them with medicinal aluminum foil (YBB00152002-2015) of the same size. Heat seal on a heat sealer at a temperature of 150 ℃± 5 ℃, a pressure of 0.4MPa, and a time of 1 second. According to the heat sealing strength determination method (YBBOO122003-2015), it shall not be lower than 7.0N/15mm

[Thickness] Specification size 0.20-0.40mm, allowable deviation ± 0.02

Jinan Sanquan Zhongshi Experimental Instrument Co., Ltd., a pharmaceutical packaging material enterprise, has produced heat shrink testers, heat sealers, intelligent electronic tensile testing machines, pharmaceutical packaging tearing force testers, thickness gauges, drop ball impact testers, water vapor permeability testers, etc. in accordance with YBB00212005-2015 "Polyvinyl Chloride Solid Medicinal Hard Tablets" regulations.