- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/10/2013)
- Gwreiddiol (a wnaed Fel)
Version Superseded: 17/05/2024
Point in time view as at 01/10/2013. This version of this provision has been superseded.
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There are currently no known outstanding effects for the The Veterinary Medicines Regulations 2013, Paragraph 3.
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3. The summary of product characteristics required under the preceding paragraph must include the following information, set out in the same format—
Summary of product characteristics | ||
1 | Name of the veterinary medicinal product, followed by its strength and pharmaceutical form. | |
2 | The name and proportion of each active substance, and of any excipient if knowledge of the excipient is needed for safety reasons. | |
3 | Pharmaceutical form. | |
4 | Clinical particulars— | |
4.1 | target species; | |
4.2 | indications for use, specifying the target species; | |
4.3 | contra-indications; | |
4.4 | special warnings for each target species; | |
4.5 | special precautions for use, including special precautions to be taken by the person administering the medicinal product to the animals; | |
4.6 | adverse reactions (frequency and seriousness); | |
4.7 | use during pregnancy, lactation or lay; | |
4.8 | interaction with other medicinal products and other forms of interaction; | |
4.9 | amounts to be administered and administration route; | |
4.10 | overdose (symptoms, emergency procedures, antidotes) if necessary; | |
4.11 | withdrawal periods for the various foodstuffs, including those for which the withdrawal period is zero. | |
5 | Pharmacological properties— | |
5.1 | pharmacodynamic properties; | |
5.2 | pharmacokinetic particulars; | |
6 | Pharmaceutical particulars— | |
6.1 | list of excipients; | |
6.2 | major incompatibilities; | |
6.3 | shelf life, when necessary after reconstitution of the medicinal product or when the immediate packaging is opened for the first time; | |
6.4 | special precautions for storage; | |
6.5 | nature and contents of immediate packaging; | |
6.6 | special precautions for the disposal of unused veterinary medicinal products or waste materials derived from the use of such products, if appropriate; | |
7 | Marketing authorisation holder; | |
8 | Marketing authorisation number; | |
9 | Date of the first authorisation or date of renewal of the authorisation; | |
10 | Date of any revision of the text; | |
11 | Any other information required by the Secretary of State. |
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Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
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