氨咖黄敏胶囊对乙酰氨基酚检测评价数据

为保证氨咖黄敏胶囊安全性，需要对该胶囊中对乙酰氨基酚含量进行把控，该含量内控指标为95.0%-105.0%（高于药典标准）。本数据主要用于检测氨咖黄敏胶囊含量指标的情况，为企业管控产品质量提供数据支持。1、数据采集：数据采集于公司产品。 2、计算公式：对乙酰氨基酚含量=(V*F*15.12*T)/(0.25*W*1000)，其中V为消耗滴定液容积，F为校正因子，T为供试品平均装量，W为供试品重量。3、将以上监测数据对比内控标准要求，超出限定值为不合格。标准值范围内为合格。4、检验氨咖黄敏胶囊中对乙酰氨基酚含量，不仅仅检验该药品的质量，更可以为企业在生产氨咖黄敏胶囊过程中的工艺、设备以及原材料质量提供参考依据。

To ensure the safety of Paracetamol, Caffeine, Artificial Calculus Bovis and Chlorphenamine Maleate Capsules, it is imperative to control the paracetamol content within these capsules, with the internal control limit set at 95.0%-105.0% (higher than the pharmacopoeial standard). This dataset is primarily used to detect the paracetamol content index of the aforementioned capsules, providing data support for enterprises to manage and control product quality.
1. Data Collection: The data is collected from the company's manufactured products.
2. Calculation Formula: The paracetamol content is calculated as (V × F × 15.12 × T) / (0.25 × W × 1000), where V is the volume of consumed titrant, F is the correction factor, T is the average fill weight of the test samples, and W is the weight of the test sample.
3. Qualification Judgment: Compare the above monitoring data with the internal control limits. Samples with content exceeding the limit are deemed unqualified, while those within the standard range are qualified.
4. Supplementary Value: Detecting the paracetamol content in Paracetamol, Caffeine, Artificial Calculus Bovis and Chlorphenamine Maleate Capsules not only verifies the quality of the pharmaceutical product, but also provides reference basis for enterprises to optimize production processes, maintain equipment and control raw material quality during the manufacturing of these capsules.

搜集汇总

数据集介绍

特点

该数据集包含氨咖黄敏胶囊中对乙酰氨基酚含量的检测评价数据，共601条记录，每年更新一次，用于企业产品质量管控，确保含量符合内控标准。