N.M. Admin. Code § 16.19.8.19

Current through Register Vol. 35, No. 19, October 8, 2024

Section 16.19.8.19 - REPACKAGER LICENSING REQUIREMENTS

A. Every repackager, wherever located, who engages in distribution into, out of, or within this state must be licensed by the board in accordance with the laws and regulations of this state before engaging in repackaging or distribution of prescription drugs.

B. A repackager shall have valid registration with the FDA as a drug establishment under section 510 of the Federal Act.

C. Repackagers cannot operate from a place of residence.

D. Where repackaging operations are conducted at more than one location, each such location shall be licensed by the board.

E. The repackaging facility shall be located apart and separate from any pharmacy licensed by the board.

N.M. Admin. Code § 16.19.8.19

Adopted by New Mexico Register, Volume XXVIII, Issue 22, November 28, 2017, eff. 11/28/2017