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Directive 2001/82/EC of the European Parliament and of the CouncilShow full title
Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products
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Revised version PDFs
- Revised 07/08/20090.89 MB
- Revised 20/07/20090.40 MB
- Revised 06/03/20090.37 MB
- Revised 30/04/20040.35 MB
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Changes over time for: Article 59
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Article 59U.K.
[F11. As regards ampoules, the particulars listed in the first paragraph of Article 58(1) shall be given on the outer package. On the immediate packaging, however, only the following particulars shall be necessary:]
name of veterinary medicinal product,
quantity of the active substances,
route of administration,
manufacturer's batch number,
date of expiry,
the words ‘For animal treatment only’.
[F12. As regards small immediate packaging containing a single dose, other than ampoules, on which it is impossible to give the particulars mentioned in paragraph 1, the requirements of Article 58(1), (2) and (3) shall apply only to the outer package.
3. The particulars mentioned in the third and sixth indents of paragraph 1 shall appear on the outer package and on the immediate packaging of the medicinal products in the language or languages of the country in which they are placed on the market.]
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