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Commission Delegated Regulation (EU) 2016/161 ANNEX III

Commission Delegated Regulation (EU) 2016/161 ANNEX III

ANNEX IIISupplementary provisions

ANNEX III Notification to the European Commission of medicinal products not subject to prescription judged 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 Supporting Evidence (please provide evidence of one or more incidents of falsification in the legal supply chain and specify the source of the 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 III 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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