Clarithromycin Olikla 500mg


Powder for concentrate for solution for infusion 10 vials

Clarithromycin Olikla 500mg


Powder for concentrate for solution for infusion 10 vials
Registered name:
Clarithromycin Olikla  
Registration number 15/133/18-C
SUKL code 0266384
Date of first registration / renewal 6. 5. 2021
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Anfarm Hellas S.A., 61 st km Nat.rd. Athens Lamia, Schimatari, Viotias, 32009 Greece

  • Active substance

    Each vial contains 500 mg clarithromycin.
  • Excipients with known effect

    Sodium hydroxide
  • Therapeutic area

    Antibiotics
  • Pharmacotherapeutic group

    Antibacterial for systemic use, macrolide
  • ATC group

    J01FA09
  • Dosage form

    Powder for concentrate for solution for infusion
  • Route of administration

    Intravenous admnistration
  • Storage conditions

    This medicinal product does not require any special storage conditions.
  • Expiration

    3 years
  • Reimbursement from health insurance companies

    Prescription only medicine. Fully paid.
  • Current availability in the Czech market and delivery time

    Yes, on the stock in CR
  • EAN

    8594184140963
  • PDK code

    4782836

QR code for PIL / QR code for SPC

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Dear Madam, Dear Sir,
Please note that the Olikla website you are accessing is not intended for the general public because it contains expert information on drugs and medical devices, including advertising messages, relating to drugs and medical devices. These messages and information are solely for professionals under Section 2a of Act No. 40/1995 Coll., on Regulation of Advertising, as amended, i.e. persons authorised to prescribe or dispense drugs or medical devices (“professionals”).

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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