Drug · DIN 00690791
RATIO-MORPHINE
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since May 18, 2018; first marketed December 31, 1986.
- Drug Identification Number (DIN)
- 00690791
- Company (DIN owner)
- Teva Canada LimitedToronto, Ontario, Canada
- Schedule
- Narcotics (CDSA I)
- Dosage form
- Syrup
- Route
- Oral
- Therapeutic class (ATC)
- Morphine N02AA01
- Class
- Human
- Record last updated
- June 12, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| MORPHINE HYDROCHLORIDE | 20 MG | ML |
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “ratio-morphine”. A notice may cover another product or only some lots: read it to see what it covers.
- Ratio-Morphine Tablets Recalled in Canada due to Risk of Accidental Overdose - For Health ProfessionalsJuly 14, 2008 · Drugs
- Archived – Ratio-Morphine Tablets Recalled in Canada due to Risk of Accidental OverdoseJuly 9, 2008 · Drugs · Dosage - Labelling
Other DINs named RATIO-MORPHINE
- DIN 00607762 · Cancelled Post Market
- DIN 00607770 · Cancelled Post Market
- DIN 00690783 · Cancelled Post Market