This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Supeudol 20
- Starting date:
- April 5, 2013
- Posting date:
- April 23, 2013
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-26855
Recalled Products
- Supeudol 20
Reason
The recall is initiated following an out-of-specification result for the assay of oxycodone hydrochloride obtained in stability (6 month time point).
Depth of distribution
Wholesalers and pharmacies in Canada.
Affected products
A. Supeudol 20
DIN, NPN, DIN-HIM
DIN 00392472
Dosage form
- Suppository
Strength
- 20 mg
Lot or serial number
- 133429A
Companies
- Recalling Firm
-
Sandoz Canada Inc.
145 Jules-Léger
Boucherville
J4B 7K8
Quebec
CANADA
- Marketing Authorization Holder
-
Sandoz Canada Inc.
145 Jules-Léger
Boucherville
J4B 7K8
Quebec
CANADA