Ceftazidime Olikla 1g


powder for solution for injection/infusion 10 vials

Ceftazidime Olikla 1g


powder for solution for injection/infusion 10 vials
Registered name:
Ceftazidime Olikla 
Registration number 15/300/22-C
SUKL code 0279311
Date of first registration / renewal 14.5.2024
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Kymos S.L., Ronda de Can Fatjó, 7B (Parque Tecnológico del Vallés), Cerdanyola del Vallés, 08290 Barcelona, Spain
Producer Eurofins Analytical Services Hungary Kft., Anonymus u. 6, 1045 Budapešť, Hungary

  • Active substance

    Each vial contains ceftazidime 1g (as pentahydrate). 

  • Excipients with known effect

    Sodium carbonate (anhydrous sterile). Each gram of ceftazidime contains approximately 52mg (2.3mmol) of sodium.

  • Therapeutic area

    Antibiotics
  • Pharmacotherapeutic group

    Antibacterials for systemic use. Third-generation cephalosporins.
  • ATC group

    J01DD02
  • Dosage form

    Powder for solution for injection or infusion (Powder for injection or infusion).

  • Route of administration

    Intramucsular or intravenous administration
  • Storage conditions

    Store in the original package in order to protect from light.
  • Expiration

    2 years
  • Reimbursement from health insurance companies

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

    No
  • EAN

    8594184140567
  • PDK code

    5224317

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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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