Manufacturers and repackagers inventory records shall contain the following information:

1. A. Finished form:

   1. (1) name of substance;
   2. (2) each finished form of the substance (10 milligram tablet, etc.)
   3. (3) the number of units or volume of each finished form in each commercial container (100 tablet bottle, etc.)
   4. (4) the number of commercial containers of each such finished form.
2. B. Controlled substances not included above such as damaged, defective impure substances awaiting a disposal giving total quantity and the name of the substance. A statement of reason for the substance being included in this category.

[16.19.20.21 NMAC - Rp 16.19.20.21 NMAC, 6/26/2018]