If a person manufactures, packs or distributes a drug at a place other than his principle place of business, the label may state the principle place of business in lieu of the actual place where such drug is manufactured or packed or is to be distributed, unless such statement would be misleading.

[03-07-80...08-27-90; Rn, 16.19.9.15.1, 03-14-98; 16.19.9.14 NMAC – Rn, 16 NMAC 19.9.14, 03-30-02]

History of 16.19.9 NMAC:

Pre-NMAC History:

Material in this part was derived from that previously filed with the commission of public records - state records center and archives as:

Regulation No. 9, Minimum Standards for Manufacturers and Repackaging, filed 02-07-80;

Regulation No. 9, Minimum Standards for Manufacturers and Repackaging Firms, filed 10-23-85;

Regulation No. 9, Minimum Standards for Manufacturers and Repackaging Firms, filed 02-02-87;

Regulation No. 9, Minimum Standards for Manufacturers and Repackaging Firms, filed 07-27-90.

History of Repealed Material:

16 NMAC 19.9, Minimum Standards for Manufacturers and Repackaging Firms, filed 03-03-98.

Other History:

Regulation No. 9, Minimum Standards for Manufacturers and Repackaging Firms, filed 07-27-90 renumbered and reformatted to 16 NMAC 19.9, Minimum Standards for Manufacturers and Repackaging Firms, filed 02-02-96;

16 NMAC 19.9, Minimum Standards for Manufacturers and Repackaging Firms, filed 03-03-98 - replaced by 16.19.9 NMAC, Minimum Standards for Manufacturers and Repackaging Firms, effective 06-27-01.