Amoxicillin/Clavulanic Acid Olikla


1000mg/200mg powder for solution for injection/infusion 50 vials

Amoxicillin/Clavulanic Acid Olikla


1000mg/200mg powder for solution for injection/infusion 50 vials
Registered name:
Amoxicillin/Clavulanic Acid Olikla 
Registration number 15/ 001/20-C
SUKL code 0264611
Date of first registration / renewal 21.12.2021
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Laboratorio Reig Jofré S.A., Jarama 111, Polígono Industrial, 45007 Toledo, Spain

  • Active substance

    One vial contains amoxicillinum 1000 mg (as amoxicillinum natricum) and acidum clavulanicum 200 mg (as potassiumi clavulanas).
  • Excipients with known effect

    The sodium content of each vial is 2.7 mmol. The potassium content of each vial is 1.0 mmol.
  • Therapeutic area

    Antibiotics
  • Pharmacotherapeutic group

    Combinations of penicillins, including of beta-lactamase inhibitors
  • ATC group

    J01CR02
  • Dosage form

    Powder for solution for injection/infusion.
  • Route of administration

    Intravenous use.
  • Storage conditions

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

    3 years
  • 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

    8594184140932
  • PDK code

    4715216

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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.

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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.

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