`en
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`European Commission
`Public Health
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`European Commission Public health Reference documents Community Register of medicinal products
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`PHARMACEUTICALS - COMMUNITY
`REGISTER
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`
`
`Print version
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`See for information on RSS news feeds for the Community Register
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`
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`Frequently asked Questions
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`Procedures for centrally authorised medicinal products1
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`Community Register of medicinal products for human use2
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`Active
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`Withdrawn, suspended, expired or not
`renewed
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`By EU number
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`By EU number
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`Refused
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`Alphabetical
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`Alphabetical
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`Alphabetical
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`Community Register of orphan medicinal products for human use3
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`Active
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`Withdrawn or expired
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`Refused
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`By EU number
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`By EU number
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`
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`Community Register of veterinary medicinal products4
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`Active
`
`Withdrawn, suspended, expired or not
`renewed
`
`By EU number
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`By EU number
`
`Refused
`
`
`
`Alphabetical
`
`Alphabetical
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`Alphabetical
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`Alphabetical
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`Alphabetical
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`Alphabetical
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`Procedures for nationally authorised medicinal products
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`Medicinal products for human use
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`Veterinary medicinal products
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`
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`
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`Alphabetical
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`Alphabetical
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`5
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`WATSON LABORATORIES, INC. , IPR2017-01622, Ex. 1038, p. 1of 2
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`
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`List medicinal products authorised under Article 126a
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`Adopted Commission Decisions of the last six months
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`Human medicinal products by ATC
`Veterinary medicinal products by ATC
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`General index on active ingredient
`General index on brand name
`General index on Marketing Authorisation Holders and Sponsors
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`Subscriptions to RSS news feeds
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`1
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`2
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`3
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`4
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`5
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`Variation procedures which do not affect the Commission Decision granting the marketing authorisation (including its
`annexes) are no longer reflected in the Community Register of medicinal products since 1 April 2011.
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`The Register of medicinal products for human use authorised by the EU under the centralised procedure. Published in
`accordance with Article 13 of Regulation (EC) No 726/2004 .
`
`The Register of orphan medicinal products for human use designated and published by the EU in accordance with
`Article 5 of Regulation (EC) N141/2000.
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`The Register of veterinary medicinal products authorised by the EU under the centralised procedure. Published in
`accordance with Article 38 of Regulation (EE) 726/2004.
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`The list of Exceptional Marketing Authorisations is published in accordance with Article 126a of Directive 2001/83/EC
`of the European Parliament and of the Council of 6 november 2001 on the community code relating to medicinal
`products for human use
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`CONTACT
`
`Directorate General Health &
`Consumers
`
`General information enquiries
` Call 00 800 6 7 8 9 10 11
` E-mail your questions
`
`Last update: 23/02/2017 | Top
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`WATSON LABORATORIES, INC. , IPR2017-01622, Ex. 1038, p. 2of 2
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