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Ranitidine-150 (November 25, 2011)

Starting date:
November 25, 2011
Posting date:
December 28, 2011
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-2011A201

Reason

Good manufacturing practices (GMP) deficiencies. The recalled Ranitidine-150 lots were not manufactured as per the approved Pro Doc master batch record.

Depth of distribution

Wholesalers, retailers in Quebec

Affected products

Ranitidine-150

DIN, NPN, DIN-HIM

DIN 00740748

Dosage form

Tablets

Strength

  • 150 mg

Lot or serial number

5109, 5109-1, 5157, 5158

Companies

Recalling Firm
Pro-Doc Ltd.
2925 Industrial Blvd.
Laval Quebec
Canada
Marketing Authorization Holder
Pro-Doc Ltd.
2925 Industrial Blvd.
Laval Quebec
Canada