Título 26. FOOD, DRUGS, AND COSMETICS · Capítulo 3. STANDARDS, LABELING, AND ADULTERATION OF DRUGS AND COSMETICS
26-3-9. Name and address of manufacturer on label of drugs requiring prescription.
Actualizado hasta: Including Acts of the 2025 Regular Session of the General Assembly.
El texto siguiente es la ley tal como la imprime el estado, en inglés.
- (a)
Any drug product designed for human usage which is branded as follows:#
“Caution: Federal law prohibits dispensing without prescription”
shall bear on the label the name and address of the manufacturer.
- (b)
For the purposes of this Code section, the term “manufacturer” includes any of the following parties:#
- (1)
The person who is responsible for the production of the drug and maintains control over the processing of same;#
- (2)
The person to whose specifications the drug is manufactured and who reviews adherence to such specifications through a drug testing program;#
- (3)
The person who manufactures the drug product and then packs and ships the said drug products on behalf of the person designated on the label as being responsible for the drug product; or#
- (4)
The person who manufactures the drug product and which product is distributed by the person designated on the label as being responsible for the drug without testing to determine adherence to specifications for manufacture.#
- (c)
Where the drug product is manufactured by an affiliated or subsidiary company of the distributor, the name and address of the distributor only need appear.#
History
Code 1933, § 79A-1009.1, enacted by Ga. L. 1975, p. 691, § 1; Ga. L. 1982, p. 3, § 26.
Leer la página oficial (el PDF del estado, abierto en la página de la que se leyó este texto).
Actualizado hasta: Including Acts of the 2025 Regular Session of the General Assembly.
Texto leído de t24-t26-(v21)-2023-pdf.pdf, Volumen V21, edición 2023, páginas 471 a 472; acción de fusión: carried; SHA-256 del archivo 8eab3bec6887.