N.M. Code R. § 16.19.21.35
Controlled Substance Precursors
The following substances are designated as immediate precursors used in the manufacture of controlled substances:
- A. phenyl acetone;
- B. ephedrine;
- C. phenyl-2-propanone;
- D. norephedrine;
- E. ethyl-1-methyl butyl diethyl malonate;
- F. allyl-1-methyl butyl diethyl malonate;
- G. hydroxyindole;
- H. 3,4,5-trimethoxybenzyl cyanide;
- I. 3,4,5-trimethoxybenzyl alcohol;
- J. 3,4,5-trimethoxyphenylacetonitraile;
- K. 3,4,5-trimethoxybenzoic acid amide;
- L. 4-benzyloxyindole;
- M. 4-chloro indole;
- N. indole;
- O. tryntophol;
- P. 3-indole glyoxylic acid;
- Q. 3-indole glyoxylic acid ethyl ester;
- R. lysergic acid;
- S. lysergic acid amide;
- T. ergotamine tartrate;
- U. 1-phenyl cyclohexylamine;
- V. 1-piperidinocyclohexanecarbonitrile;
- W. pseudoephedrine as a substance in a form not approved in 26-1-14 NMSA;
- X. methylamine;
- Y. methylformamide
Z. phenylacetic acid;
AA. anhydrous ammonia:
(1) a person shall not possess any amount of anhydrous ammonia;
(2) a person must store anhydrous ammonia in a container approved for the transport of anhydrous ammonia;
(3) the provisions of this section do not apply to a:
(a) person who is actively operating land used for agricultural purposes;
(b) retail distributor;
(c) wholesaler;
(d) manufacturer;
(e) warehouseman;
(f) common carrier; or
(g) person engaged in the regular course of conducting a lawful business;
BB. red phosphorous;
CC. iodine matrix, a retail distributor registrant, pharmacy, hospital, clinic may not sell more than 2 ounces of iodine matrix in a single transaction;
DD. crystal iodine, a retail distributor registrant, pharmacy, hospital, clinic may not sell more than 2 ounces of iodine crystals in a single transaction.
[03-07-80…08-27-90; 16.19.21.35 NMAC - Rn, 16 NMAC 19.21.35, 03-30-02; A, 12-01-03; A, 01-15-2005; A, 01-31-07
HISTORY OF 16.19.21 NMAC:
Pre-NMAC History: The material in this part was derived from that previously filed with the State Records Center and Archives:
Regulation No. 21, Drug Precursors, 8-28-89.
Regulation No. 21, Drug Precursors, 7-27-90.
History of Repealed Material: [RESERVED]
Other History: 16 NMAC 19.21, Pharmacists - Drug Precursors, filed 02-02-96, reformatted and renumbered to 16.19.21 NMAC, Drug Precursors, effective 03-30-2002.