LOETTE

Main information

  • Trade name:
  • LOETTE Film-coated tablet 0,1MG/0,02MG
  • Dosage:
  • 0,1MG/0,02MG
  • Pharmaceutical form:
  • Film-coated tablet
  • Administration route:
  • Oral use
  • Units in package:
  • 1X28 II Blister
  • Prescription type:
  • with prescription
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • LOETTE Film-coated tablet 0,1MG/0,02MG
    Czech Republic
  • Language:
  • English

Therapeutic information

  • Therapeutic area:
  • LEVONORGESTREL AND ETHINYL ESTRADIOL
  • Product summary:
  • LOETTE

Other information

Status

  • Source:
  • SUKL - Státní ústav pro kontrolu léčiv
  • Authorization status:
  • R - active MA/authorised medicinal product
  • Authorization number:
  • 17/ 492/99-C
  • Last update:
  • 13-07-2018

There are no safety alerts related to this product.