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0019.939764
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008240624t20242024onc     o    f000 0 eng d
020 |a9780660725031
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-273/1-2024E-PDF
24500|aGuidance document : |bregulatory requirements for drug identification numbers (DINs).
24617|aRegulatory requirements for drug identification numbers (DINs)
250 |a[2024/07/15 edition].
264 1|aOttawa, Ontario : |bHealth Canada = Santé Canada, |c2024.
264 4|c©2024
300 |a1 online resource (35 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aCover title.
500 |a"Publication date: July 2024."
500 |a"Date adopted: 2019/05/03 ; Effective date: 2019/05/03 ; Administrative changes date: 2024/07/15."
500 |aIssued also in French under title: Ligne directrice : exigences réglementaires associées à une identification numérique attribuée à une drogue (DIN).
520 |a"When Health Canada authorizes a drug to be marketed in Canada, a Drug Identification Number (DIN) is assigned to the manufacturer and printed on the package labels. A DIN indicates that the evaluation of the drug determined that it met the relevant requirements of the Food and Drugs Act and its Regulations and the drug has a favourable risk/benefit profile. Manufacturers of prescription and non-prescription drugs must obtain a DIN before they are marketed in Canada. Market authorization of a drug may require the additional issuance of a Notice of Compliance (NOC)"--Introduction, page 10.
650 0|aDrugs|xLabeling|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLigne directrice : |w(CaOODSP)9.939767
795 |tGuidance document : |b[2024/05/01 edition]|w9.936452
85640|qPDF|s501 KB|uhttps://publications.gc.ca/collections/collection_2024/sc-hc/H164-273-1-2024-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/regulatory-requirements-drug-identification-numbers/document.html