Micafungin Olikla 1x100mg


powder for concentrate for solution for infusion

Micafungin Olikla 1x100mg


powder for concentrate for solution for infusion
Registered name:
Micafungin Olikla  
Registration number 26/ 224/19-C
SUKL code 0239446
Date of first registration / renewal 21. 07. 2020
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Galenicum Health, S.L., Avda, Corenellá 144, Edificio Lekla, Esplugues de Llobregat 08950, Barcelona, Spain
Producer SAG Manufacturing S.L.U., Ctra. N-I, Km 36, San Augustin de Guadalix, 28750, Madrid, Spain

  • Active substance

    Each vial contains 100 mg micafungin (as sodium).
  • Excipients with known effect

    Lactose monohydrate, citric acid, sodium hydroxide
  • Therapeutic area

    Antifungals
  • Pharmacotherapeutic group

    Antimycotics for systemic use
  • ATC group

    J02AX05
  • Dosage form

    Powder for concentrate for solution for infusion
  • Route of administration

    Intravenous administration
  • Storage conditions

    Keep the bottle in the outer carton in order to protect from light.
  • Expiration

    30 months
  • Reimbursement from health insurance companies

    Prescription only medicine. Partially covered.
  • Current availability in the Czech market and delivery time

    Yes, on the stock in CR
  • EAN

    8594184140260
  • PDK code

    3997484

QR code for PIL / QR code for SPC

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Please note that if you are not a professional, you risk endangering your health or the health of others if you misunderstand or misinterpret the information obtained, in particular the advertising messages which may be part of this website, or use it for self-diagnosis or the determination of medical treatment, whether in relation to you personally or in relation to others.

I declare that I have acquainted myself with the above advice, including the definition of a professional, and I am aware of the risks a person other than a professional accessing this website is exposed to.

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Dear Madam, Dear Sir,
In the previous step, you confirmed you are a professional as defined by Act No. 40/1995 Coll., on Regulation of Advertising, as amended, i.e. that you are a person authorised to prescribe or dispense drugs and medical devices. If your declaration is untrue, please note that you are endangering your health or the health of others.

YES, I declare I am a professional under Section 2a of Act No. 40/1995 Coll., on Regulation of Advertising.

NO, I am not a professional under Section 2a of Act No. 40/1995 Coll., on Regulation of Advertising.

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