White Paper on Guidelines on the Labelling of Pharmaceutical Products

Published in 2009 by the Department of Health, Pharmaceutical Service, China, this report clarifies labelling requirements in respect of pharmaceutical products for the purpose of registration.

The paper states that for general labelling requirements the products must contain: name of the product, name and quantity of each active ingredient, manufacturer's name and address, Hong Kong registration number of the product, batch number, expiry date and specific storage conditions, if any.

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