Non-prescription Drugs: Labelling Standards - Drug Product
Labelling standards are developed for drugs that have a well characterized safety and efficacy profile under specific conditions of use. A manufacturer may reference a labelling standard in a drug submission when the product and its labelling are consistent with the information set out in the document.
- Publisher
- Health Canada
- Resources
- 2
- Catalogue metadata updated
- 2021-09-09
Data overview
- Formats
- HTML
- File languages
- English, French