How to Record the Packaging Specifications of Drugs as Prescribed?

How is the packaging specification of pharmaceuticals regulated?Dear Editorial Board of Legal Secretary, I have a question as follows: I work in market management, mainly dealing with pharmaceutical management activities. Currently, there are many types of drugs and functional products that violate labeling regulations. Now I would like to ask: How is the packaging specification of pharmaceuticals regulated? What contents does it include? And which legal document regulates this? I hope the Editorial Board of Legal Secretary can answer my question. Thank you!Nhat Ha, Hanoi.

According to Clause 2, Article 28 of Circular 01/2018/TT-BYT, the packaging specifications for medicines are as follows:

- The packaging specifications are recorded in natural numbers regarding the quantity, weight, and volume of the medicine contained within the commercial packaging;

- In cases where a commercial packaging of the medicine contains multiple packaging units, the specific quantity of each packaging unit and the total packaging units must be recorded;

- Clearly record other components accompanying the medicine, such as: needles, syringes, measuring spoons, measuring cups, nebulizer equipment, and other auxiliary tools included in the commercial packaging of the medicine (if any).

Note: For medicines listed under special control categories such as narcotic drugs, psychotropic drugs, and drugs containing precursors, the outer packaging of the medicine must not contain more than 100 smallest packaging units.

Respectfully!

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