The following particulars with regard to applications for registration referred to in section 15(10) of the Act shall be published in the Gazette:
| (a) | The proprietary name of the medicine; |
| (b) | the approved name and quantity of each active ingredient of the medicine contained in a dosage unit or per suitable mass or volume or unit; |
| (c) | the dosage form of the medicine; |
| (d) | the name of the applicant who lodged the application for registration; |
| (e) | the number allocated to it in terms of section 15 of the Act; |
| (f) | the name and address of the manufacturer; |
| (g) | the name of the person responsible for the final product release control; and |
| (h) | name of the person responsible for final product release responsibility. |
