Pantoprazol Olikla 40mg


powder for solution for injection 10 vials

Pantoprazol Olikla 40mg


powder for solution for injection 10 vials
Registered name:
Pantoprazol Olikla  
Registration number 09/622/16-C
SUKL code 0136834
Date of first registration / renewal 17.1.2018
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Laboratorios Normon S.A., Ronda de Valdecarrizo 6, 28760 Tres Cantos, Madrid, Spain

  • Active substance

    Each vial contains 40 mg of pantoprazole (as sodium sesquihydrate)
  • Excipients with known effect

    Disodium edetate dihydrate

  • Therapeutic area

    Gastroenterology
  • Pharmacotherapeutic group

    Proton pump inhibitors
  • ATC group

    A02BC02
  • Dosage form

    Powder for injection for solution
  • Route of administration

    Intravenous administration
  • Prescribing restrictions

    No
  • Indication restriction

    No
  • Storage conditions

    Store below 30 °C.
  • 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

    8594184140086
  • PDK code

    3588101

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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