Quality Review of Documents Product Information Templates
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Quality Review of Documents Product Information Template
This medicine is authorised in the Member States of the European Economic Area
under the following names:
Identifier
200000029918
Term Name
en
bg
cs
da
de
el
es
et
fi
fr
ga
hr
hu
is
it
lt
lv
mt
nl
no
pl
pt
ro
sk
sl
sv
This medicine is authorised in the Member States of the European Economic Area
under the following names:
Translation Status
CURRENT
Modified on
2024-08-27
Status
CURRENT
Domain
Human use - H
Parent
6. Contents of the pack and other information
Hierarchy
This medicine is authorised in the Member States of the European Economic Area
under the following names:
(level=H3)
/
6. Contents of the pack and other information
(level=H2)
/
PACKAGE LEAFLET
(level=H1)
Data Classification
PUBLIC
Extended Attributes
Is blank subsection allowed
N
Is Mandatory
N
Product Information Document Type
Package Leaflet - pl
Regulatory Authorisation/Registration Procedure
Decentralised Procedure - DCP
Regulatory Authorisation/Registration Procedure
Mutual Recognition Procedure - MRP
Regulatory Authorisation/Registration Procedure
National Procedure - NP
Sequence Order
128
