Co-Codamol 30 500mg Tablets UKPAR

1 Co-Codamol 30/ 500mg Tablets . PL 04077/0224. UKPAR . TABLE OF CONTENTS. Lay Summary Page 2. Scientific discussion Page 3. Steps taken for assessment Page 10. Steps taken after authorisation summary Page 11. Summary of Product Characteristics Page 12. Product Information Leaflet Page 27. Labelling Page 29. MHRA PAR Co-Codamol 30/ 500mg Tablets -1- Co-Codamol 30/ 500mg Tablets . PL 04077/0224. LAY SUMMARY. The MHRA granted M and A Pharmachem Limited a Marketing Authorisation (licence). for the medicinal product Co-Codamol 30/ 500mg Tablets (PL 04077/0224) on 5th June 2006. This prescription-only medicine is for the relief of severe pain.

2 Co-Codamol 30/ 500mg Tablets contains the active ingredients codeine phosphate and paracetamol which act as analgesics. This application is an abridged simple application of a previously granted application, Co- codamol 30/ 500mg Tablets BP, which were initially granted a UK licence on 16th August 2004. No new or unexpected safety concerns arose from this simple application and it was, therefore, judged that the benefits of taking Co-Codamol 30/ 500mg Tablets outweigh the risks, hence, a Marketing Authorisation has been granted. MHRA PAR Co-Codamol 30/ 500mg Tablets -2- Co-Codamol 30/ 500mg Tablets .

3 PL 04077/0224. SCIENTIFIC DISCUSSION. TABLE OF CONTENTS. Introduction Page 4. Pharmaceutical assessment Page 5. Preclinical assessment Page 7. Clinical assessment Page 8. Overall conclusions and risk benefit assessment Page 9. MHRA PAR Co-Codamol 30/ 500mg Tablets -3- INTRODUCTION. The UK granted marketing authorisations for the medicinal product Co-Codamol 30/ 500mg Tablets to M and A Pharmachem on 5th June 2006. The product is a prescription- only medicine (POM). The application was submitted as a simple abridged application according to Article 10c (formerly (a)(i)) of Directive 2001/83/EC, cross-referring to Co-Codamol 30/ 500mg Tablets BP (PL 04077/0186), which was initially granted a licence in August 2004.

4 No new data were submitted nor were they necessary for this simple application, as the data are identical to that of the previously granted cross-reference product. As the cross- reference product was granted prior to the introduction of current legislation, no public assessment report (PAR) was generated for it. The product contains the active ingredients codeine phosphate and paracetamol which act as analgesics. Co-Codamol 30/ 500mg Tablets are indicated for the relief of severe pain. MHRA PAR Co-Codamol 30/ 500mg Tablets -4- PHARMACEUTICAL ASSESSMENT. LICENCE NO: PL 04077/0224.

5 PROPRIETARY NAME: Co-Codamol 30/ 500mg Tablets ACTIVE(S): Codeine Phosphate and Paracetamol COMPANY NAME: M and A Pharmachem Limited ARTICLE: Article 10c of Directive 2001/83/EC, as amended LEGAL STATUS: POM. 1. INTRODUCTION. This is a simple, piggy back application for Co-Codamol 30/ 500mg Tablets submitted under Article 10c of Directive 2001/83/EC, as amended. The proposed MA holder is M and A Pharmachem Limited, Allenby Laboratories, Wigan Road, Westhoughton, Bolton, Lancashire, UK, BL5 2AL. This application cross refers to a standard abridged application for Co-Codamol 30/ 500mg Tablets BP (PL 04077/0186), which is currently registered in the UK.

6 This application is considered valid. 2. MARKETING AUTHORISATION APPLICATION FORM. Name(s). The proposed name of the product is Co-Codamol 30/ 500mg Tablets . The product has been named in line with current requirements. Strength, pharmaceutical form, route of administration, container and pack sizes The products contain codeine phosphate and paracetamol, equivalent to 30mg and 500mg , respectively. They are to be stored in aluminium/PVC strips in pack sizes of 10, 20, 30, 50. and 100 Tablets . The proposed shelf-life of 36 months is consistent with the cross-reference product.

7 The storage conditions are Do not store above 25oC. Store in the original package . These are consistent with the cross-reference product. Legal status On approval, the products will be subject to medical prescription by healthcare professionals only (POM). Marketing authorisation holder/Contact Persons/Company The proposed Marketing Authorisation holder is M and A Pharmachem Limited, Allenby Laboratories, Wigan Road, Westhoughton, Bolton, Lancashire, UK, BL5 2AL. The QP responsible for pharmacovigilance is stated and their CV is included. Manufacturers The proposed manufacturing sites are consistent with those registered for the cross- reference product and evidence of GMP compliance has been provided.

8 Qualitative and quantitative composition MHRA PAR Co-Codamol 30/ 500mg Tablets -5- The proposed composition is consistent with the details registered for the cross-reference product. Manufacturing process The proposed manufacturing process is consistent with the details registered for the cross- reference product and the maximum batch size is stated. Finished product/shelf-life specification The proposed finished product specification is in line with the details registered for the cross-reference product. Drug substance specification The proposed drug substance specification is consistent with the details registered for the cross-reference product.

9 TSE Compliance No materials of animal or human origin are included in the product. 3. EXPERT REPORTS. The applicant has included detailed expert reports in Module 2 of the application. Signed declarations and copies of the experts' CVs are enclosed in Module for the quality, non- clinical and clinical experts. All are considered to have sufficient experience for their responsibilities. 4. PRODUCT NAME & APPEARANCE. See for details of the proposed product name. The appearance of the product is identical to the cross-reference product. 5. SUMMARY OF PRODUCT CHARACTERISTICS.

10 The proposed SmPC is consistent with the details registered for the cross-reference product. 6. PATIENT INFORMATION LEAFLET/CARTON. PIL. The patient information leaflet has been prepared in-line with the details registered for the cross-reference product. Carton and blister The proposed artwork is comparable to the artwork registered for the cross-reference product and complies with statutory requirements. In line with current legislation the applicant has also included the name of the product in Braille on the outer packaging and has included sufficient space for a standard UK pharmacy dispensing label.