FML Liquifilm
FML Liquifilm is a medicine authorised by Swissmedic under authorisation number 38084. The authorisation holder is AbbVie AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 17 October 1973 and the authorisation is valid without a time limit. ATC code S01BA07 places the medicine in the group Ophthalmologicals.
| Authorisation number | 38084 |
|---|---|
| Name | FML Liquifilm |
| Full name | FML Liquifilm, Augentropfensuspension |
| Authorisation holder | AbbVie AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | S01BA07 |
| First authorisation | 17 October 1973 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | FML Liquifilm, Augentropfensuspension | A | 17 October 1973 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 11 | 5 | ml | S01BA07 | 11.06.1. | A |
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Frequently asked questions
Is FML Liquifilm authorised in Switzerland?
Yes. FML Liquifilm is authorised by Swissmedic under authorisation number 38084, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does FML Liquifilm have?
FML Liquifilm is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.
Who is the authorisation holder of FML Liquifilm?
The authorisation holder is AbbVie AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.