Venlax ER 37.5 mg
Venlax ER 37.5 mg is a medicine authorised by Swissmedic under authorisation number 59106. The authorisation holder is Drossapharm AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 04 June 2009 and the authorisation is valid without a time limit. ATC code N06AX16 places the medicine in the group Psychoanaleptics.
| Authorisation number | 59106 |
|---|---|
| Name | Venlax ER 37.5 mg |
| Full name | Venlax ER 37.5 mg, Hartkapseln, retardiert |
| Authorisation holder | Drossapharm AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | N06AX16 |
| First authorisation | 04 June 2009 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Venlax ER 37.5 mg, Hartkapseln, retardiert | B | 27 May 2010 |
| 2 | Venlax ER 75 mg, Hartkapseln, retardiert | B | 04 June 2009 |
| 3 | Venlax ER 150 mg, Hartkapseln, retardiert | B | 04 June 2009 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 7 | 7 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 1 | 14 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 2 | 28 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 3 | 98 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 4 | 14 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 5 | 28 | Kapsel(n) | N06AX16 | 01.06.0. | B |
| 6 | 98 | Kapsel(n) | N06AX16 | 01.06.0. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Venlax ER 37.5 mg authorised in Switzerland?
Yes. Venlax ER 37.5 mg is authorised by Swissmedic under authorisation number 59106, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Venlax ER 37.5 mg have?
Venlax ER 37.5 mg is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Venlax ER 37.5 mg?
The authorisation holder is Drossapharm 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.