Drug · DIN 02237829
ACID REDUCER
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 November 2, 2016; first marketed June 25, 1998.
- Drug Identification Number (DIN)
- 02237829
- Company (DIN owner)
- Mylan Pharmaceuticals UlcEtobicoke, Ontario, Canada
- Schedule
- Non-prescription drugs
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Ranitidine A02BA02
- Class
- Human
- Record last updated
- June 17, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| RANITIDINE (RANITIDINE HYDROCHLORIDE) | 75 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- October 8, 2010: NOC 11798Abbreviated New Drug Submission (ANDS) · Manufacturer name change
- March 6, 2001: NOC 2556Supplement to an Abbreviated New Drug Submission (SANDS) · Product name change from peptic relief
- April 28, 1998: NOC 3146Supplement to an Abbreviated New Drug Submission (SANDS) · New non-prescription strength
Other DINs named ACID REDUCER
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- DIN 02240348 · Cancelled Pre Market
- DIN 02241208 · Cancelled Pre Market
- DIN 02241422 · Cancelled Post Market
- DIN 02247551 · Cancelled Post Market
- DIN 02266806 · Cancelled Post Market
- DIN 02291282 · Approved
- DIN 02296160 · Dormant
- DIN 02298740 · Dormant
- DIN 02400103 · Cancelled Post Market
- DIN 02452464 · Cancelled Post Market