FLOQUIN
Main information
- Trade name:
- FLOQUIN 10 INF
- Active ingredient:
- Levofloxacin,Dextrose Anhydrous
- Available from:
- INVISION
- Dosage:
- 500MG,5%
- Pharmaceutical form:
- INF
- Composition:
- 10
- Medicine domain:
- Humans
- Medicine type:
- Allopathic drug
Documents
- for the general public:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- for healthcare professionals:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for healthcare professionals.
Localization
- Available in:
-
India
- Language:
- English
Other information
Status
- Source:
- Central Drugs Standard Control Organization
- Last update:
- 09-08-2016
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- Access to this document is only available to registered users.
Register now for full access
3-8-2018
Human medicines European public assessment report (EPAR): Cystadane, betaine anhydrous, Revision: 11, Authorised
Europe - EMA - European Medicines Agency
12-6-2018
Human medicines European public assessment report (EPAR): Quinsair, levofloxacin, Revision: 7, Authorised
Europe - EMA - European Medicines Agency
4-5-2018
Opinion/decision on a Paediatric investigation plan (PIP): , Levofloxacin (hemihydrate), Therapeutic area: Pneumology-allergology
Europe - EFSA - European Food Safety Authority EFSA Journal
11-6-2018
Quinsair (Chiesi Farmaceutici S.p.A.)
Quinsair (Active substance: levofloxacin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3756 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2789/T/16
Europe -DG Health and Food Safety