Sec. 567.001. CONTENTS OF PRESCRIPTION DRUG LABEL

(a) A prescription drug or drug product manufactured and either sold or distributed to a pharmacist in this state to be subsequently dispensed to the consumer of the drug or drug product must have affixed to the label of the drug or drug product:

(1) the name and business address of the original manufacturer of the finished dosage form; and

(2) except as provided by Subsection (b), the name and business address of each repackager or distributor of the prescription drug or drug product before delivery of the prescription drug or drug product to the pharmacist.

(b) The name and business address of a distributor is not required to be affixed as prescribed by Subsection (a) if the distributor acts only as a wholesaler or supplier and does not repackage the drug or in any way modify the individual drug package or container or the contents of the package or container as received from the manufacturer, repackager, or other distributor.

Acts 1999, 76th Leg., ch. 388, Sec. 1, eff. Sept. 1, 1999.