LODRONAT

Main information

  • Trade name:
  • LODRONAT Film-coated tablet 520MG
  • Dosage:
  • 520MG
  • Pharmaceutical form:
  • Film-coated tablet
  • Administration route:
  • Oral use
  • Units in package:
  • 60 Blister
  • Prescription type:
  • with prescription
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • LODRONAT Film-coated tablet 520MG
    Czech Republic
  • Language:
  • English

Therapeutic information

  • Therapeutic area:
  • ACID, CLODRONIC
  • Product summary:
  • LODRONAT 520

Other information

Status

  • Source:
  • SUKL - Státní ústav pro kontrolu léčiv
  • Authorization status:
  • R - active MA/authorised medicinal product
  • Authorization number:
  • 87/ 139/99-C
  • Authorization date:
  • 04-07-2014
  • EAN code:
  • 4260056111952
  • Last update:
  • 05-04-2018