Cefazolin Noridem 2g
powder for solution for injection/infusion 1 vial
Cefazolin Noridem 2g
powder for solution for injection/infusion 1 vial
|
Registered name:
Cefazolin Noridem |
|
| Registration number | 15/ 148/17-C |
| SUKL code | 0221888 |
| Date of first registration / renewal | 13. 03. 2019 / 07.09.2023 |
| Marketing authorisation holder | Noridem Enterprises Ltd, Evagorou and Makariou, Mitsi Building 3 115, 1065 Nicosia, Cyprus |
| Producer | Demo S.A., 21km National Road Athens-Lamia, 14568 Krioneri, Attiki, Greece |
-
Active substance
Each vial contains 2 g of cefazolin (as cefazolinum natricum). -
Excipients with known effect
The sodium content of each vial is 4.4 mmol.
-
Therapeutic area
Antibiotics -
Pharmacotherapeutic group
Other beta-lactam antibacterials, first-generation cephalosporins
-
ATC group
J01DB04 -
Dosage form
Powder for solution for injection/infusion -
Route of administration
Intravenous administration -
Storage conditions
Store below 30 °C.
Keep the bottle in the outer carton in order to protect from light. -
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
5208063001414 -
PDK code
3793172
Our Products
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.
Our Products
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.