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Mebeverine hydrochloride 135 mg Film-coated Tablets



Azure Pharmaceuticals LtdPA22871/006/001

Main Information

Trade NameMebeverine hydrochloride 135 mg Film-coated Tablets
Active SubstancesMEBEVERINE HYDROCHLORIDE
Dosage FormFilm-coated tablet
Licence HolderAzure Pharmaceuticals Ltd
Licence NumberPA22871/006/001

Group Information

ATC CodeA03AA04 mebeverine

Status

License statusAuthorised
Licence Issued22/11/2019
Legal statusProduct subject to prescription which may be renewed (B)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of Licence
Marketing StatusMarketed

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
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