Food and Drug Regulations
C.01.005 (1) The principal display panel of both the inner label and outer label of a drug in dosage form shall show the drug identification number assigned for that drug, preceded by the expression “Drug Identification Number” or “Drogue : identification numérique”, or both, or the abbreviation “DIN”.
(2) Subsection (1) does not apply to a drug
(a) compounded by a pharmacist pursuant to a prescription or by a practitioner; or
(b) sold pursuant to a prescription, where the label of that drug indicates:
(i) the proper name, the common name or the brand name of the drug,
(ii) the potency of the drug, and
(iii) the name of the manufacturer of the drug.
(3) For the purposes of this section and section C.01.014, a drug in dosage form means a drug in a form in which it is ready for use by the consumer without requiring any further manufacturing.
(4) and (5) [Repealed, SOR/81-248, s. 1]
- SOR/81-248, s. 1
- SOR/93-202, s. 3
- SOR/98-423, s. 2
- SOR/2001-181, s. 4
- SOR/2017-259, s. 2
- SOR/2018-69, s. 27
- Date modified: