N.M. Admin. Code § 16.19.9.7

Current through Register Vol. 35, No. 23, December 10, 2024

Section 16.19.9.7 - DEFINITIONS

For the purpose of defining Section 26-1-11 A(3) NMSA Comp. the following definitions apply:

A. "Manufacturer" means the steps in the preparation, propagation, processing or compounding of a drug - the making by chemical, physical, biological or other procedures of any articles which meet the definition of drugs and includes manipulation, sampling or control procedures resulting in the finished dosage form. Manufacture includes all the steps performed on the product itself, which do not affect intrinsically the safety, purity or potency of the product.

B. "Manufacturers" means the person or company who manufacturers a drug in its' finished dosage form.

C. "Packager" or "Packer" means a person or firm, other than a wholesaler, who distributes drugs.

D. "Distributor" means the original selling agent, other than a wholesaler, who distributes drugs.

E. "The finished dosage form" of a prescription drug is defined as that form of the drug which is or is intended to be dispensed or administered to the patient and requires no further manufacturing or processing other than packaging and labeling.

N.M. Admin. Code § 16.19.9.7

03-07-80...08-27-90; 16.19.9.7 NMAC - Rn, 16 NMAC 19.9.7 NMAC, 03-30-02