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Commission Delegated Regulation (EU) 2016/161 ANNEX IV

Commission Delegated Regulation (EU) 2016/161 ANNEX IV

ANNEX IVSupplementary provisions

ANNEX IV Notification to the European Commission of medicinal products judged not to be at risk of falsification , pursuant to article 54a(4) of Directive 2001/83/EC Member State: Name of competent authority:   Entry No Active substance (Common Name) Pharmaceutical form Strength Anatomical Therapeutical Chemical (ATC) Code Comments/Complementary information 1           2           3           4           5           6           7           8           9           10           11           12           13           14           15           Note: The number of entries is not binding.

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Other provisions in Commission Delegated Regulation (EU) 2016/161

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationANNEX IV of Commission Delegated Regulation (EU) 2016/161 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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