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What are the characteristics of the tablet medicine bottle

Jun 29 , 2021

The tablet medicine bottle is mainly used to store tablet type medicines, and can also be used to place solid medicines such as granules and capsules. Tablet drugs account for the larger category of all drugs, so what are the characteristics of the tablet medicine bottle used for its packaging?


What are the characteristics of the tablet medicine bottle

child proof bottle cap

Molnupiravir for moisture-proof packaging of drugs two requirements

medicine cap


At present, most of the tablet and medicine bottles on the market are made of polyethylene, polypropylene, polyester and other polymer materials. As raw materials for direct contact with drugs, they are non-toxic, tasteless, resistant to corrosion by most acid, alkali and solvents, and barrier Excellent performance, not fragile and other characteristics. Moreover, the weight of these raw materials is relatively light, which is convenient for transportation and convenient for patients to carry with them. The tablet medicine bottle is different from the liquid medicine packaging. Generally, the bottle mouth is slightly larger, which is more conducive to taking out the solid medicine.

In addition, the production process of tablets is to crush, granulate, and dry the materials first, and then use a tablet press to make them into tablets. Some do not need to be granulated and dried, and are directly compressed into tablets. Common tablets are ordinary tablets, coated tablets, sublingual tablets, chewable tablets, effervescent tablets, etc. These drugs are generally more resistant to moisture. If they absorb too much water, they will easily decompose and deteriorate, which will affect the efficacy and patient safety. Therefore, a desiccant is generally placed inside the tablet medicine bottle to absorb the internal water vapor to ensure the stability of the drug.

The above are the main characteristics of the tablet medicine bottle. These characteristics can protect the stability and safety of the tablet medicine during the validity period, thereby ensuring the safety of the patient.


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