Amikacin Olikla 250 mg/ml


solution for injection/infusion 1x 2ml

Amikacin Olikla 250 mg/ml


solution for injection/infusion 1x 2ml
Registered name:
Amikacin Olikla 
Registration number 15/ 281/18-C
SUKL code 0231464
Date of first registration / renewal 20.7.2021
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

    1 ml of solution for injection contains 250 mg of amikacin (as sulphate).
  • Excipients with known effect

    Sodium citrate dihydrate, sodium disulphite, sulfuric acid, water for injections.
  • Therapeutic area

    Antibiotics
  • Pharmacotherapeutic group

    Antiinfectives for systemic use, Aminoglycoside antibacterials, Other aminoglycosides
  • ATC group

    J01GB06
  • Dosage form

    Solution for injection/infusion
  • Route of administration

    Intramuscular, intravenous administration
  • Storage conditions

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

    2 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

    8594184140116
  • PDK code

    4642576

QR code for PIL / QR code for SPC

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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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