Moxifloxacin Olikla 5x 400mg


film-coated tablets

Moxifloxacin Olikla 5x 400mg


film-coated tablets
Registered name:
Moxifloxacin Olikla  
Registration number 15/924/16-C
SUKL code 0220204
Marketing authorisation holder Olikla s.r.o., Náměstí Smiřických 42, 281 63 Kostelec nad Černými lesy, Czech Republic
Producer Pharmathen S.A, Dervenakion Street 6, 15351 Pallini, Attikis, Athens, Greece
Producer Pharmathen International SA, Rodopi Prefecture, Block No 5, 69300 Rodopi, Greece

  • Active substance

    One film-coated tablet contains 400 mg moxifloxacin (as hydrochloride).
  • Excipients with known effect

    Tablet core: mannitol, colloidal anhydrous silica, microcrystalline cellulose, sodium carboxymethyl starch, hyprolose, magnesium stearate, talc. Film coating: partially hydrolysed polyvinyl alcohol, titanium dioxide (E171), macrogol, talc, yellow iron oxide (E172), red iron oxide (E172).
  • Therapeutic area

    Antibiotics
  • Pharmacotherapeutic group

    Quinolone antibacterials, fluoroquinolones
  • ATC group

    J01MA14
  • Dosage form

    Film-coated tablets
  • Route of administration

    Oral administration
  • Storage conditions

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

    5 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

    8594184140291
  • PDK code

    3674083

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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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NO, I am not a professional under Section 2a of Act No. 40/1995 Coll., on Regulation of Advertising.

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