Amoxicillin/Clavulanic Acid Olikla


1000mg/200mg powder for solution for injection/infusion 10 vials

Amoxicillin/Clavulanic Acid Olikla


1000mg/200mg powder for solution for injection/infusion 10 vials
Registered name:
Amoxicillin/Clavulanic Acid Olikla 
Registration number 15/ 001/20-C
SUKL code 0264609
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 potassium 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 beta-lactamase inhibitors
  • ATC group

    J01CR02
  • Dosage form

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

    Intravenouse 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

    4715190

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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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