When the applicant for drug registration submits supplementary application items 1, 6 and 10 in accordance with Annex 4 of the Measures for the Administration of Drug Registration, or submits supplementary application items 12 in accordance with the Provisions on the Administration of Drug Technology Transfer Registration (Note No. 518 of the State Food and Drug Administration), the relevant drug packaging materials and pharmaceutical excipients can be declared in connection with the supplementary application.