Drug · DIN 02353016
RANITIDINE
Authorized, but not sold for a year or more
Authorized, but the company reports it has not been sold in Canada for at least 12 months.
Status Dormant since July 26, 2021; first marketed July 26, 2010.
- Drug Identification Number (DIN)
- 02353016
- Company (DIN owner)
- Sanis Health Inc.Brampton, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Ranitidine A02BA02
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| RANITIDINE (RANITIDINE HYDROCHLORIDE) | 150 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- January 19, 2016: NOC 17691New Drug Submission (NDS) · Licensing agreement between two companies
- June 18, 2010: NOC 11534Abbreviated New Drug Submission (ANDS) · New manufacturer and product name
Other DINs named RANITIDINE
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- DIN 02245615 · Cancelled Pre Market
- DIN 02286106 · Cancelled Post Market
- DIN 02286114 · Cancelled Post Market
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- DIN 02303388 · Cancelled Post Market
- DIN 02343436 · Cancelled Pre Market
- DIN 02343444 · Cancelled Pre Market
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- DIN 02385961 · Cancelled Post Market