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Time and again the importance of generic prescribing has been emphasized, primarily to reduce the cost of drugs Mukherjee, There are two concepts to be understood here, one is generic vs. Non-proprietary name is the name for the active ingredient in the medicine that is decided by an expert committee and is understood internationally WHO, a. Bioequivalence is a sine qua non to generic drugs. Good quality bioequivalence studies will help to ensure safety, efficacy, and potency of a generic drug. When it is said that doctors should prescribe generic drugs, it means that they should prescribe drugs manufactured by other companies after expiry of patent of parent drug of the innovator company.

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Panadol mg Film-coated Tablets are a pain relief medication containing paracetamol. This medication also reduces fever and pain associated with colds and flu. Do not take with any other paracetamol products. Do not take more than 8 tablets in any hour period. Do not give more than 4 tablets in any hour period.

The Health Products Regulatory Authority HPRA is the Irish regulatory authority for medicinal products, medical devices and other health products including cosmetic products. The HPRA functions to protect and enhance human and animal health by approving the medicines in Ireland that meet the arimidex online canada requirements relating to quality, safety and efficacy. Medicines from other countries cannot legally be sold by non-pharmacy retailers. General sale medicines are medicines that can be sold by both non-pharmacy and pharmacy retailers. This requirement applies to both non-pharmacy and pharmacy retailers. The rationale behind the legal restrictions controlling the sale of paracetamol products is explained in the article Suicide Prevention Awareness — Health Products Regulatory Authority HPRA reminds retailers of the legal requirements when selling Paracetamol.

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