Code | 12111 | ||||||||||
MA number | EU/1/11/713/028 | ||||||||||
Product Form: | tbl flm 30x750 mg (fľ.HDPE) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Actavis Group PTC ehf., Iceland | ||||||||||
Therapeutic Class: | 21 - ANTIEPILEPTICA, ANTICONVULSIVA | ||||||||||
ATC: |
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Shelf life: | 36 | ||||||||||
Route of admin.: | Oral use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 10(1) generic application |
MA issued: | 03.10.2011 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 07.10.2020 |