Trimipramine Zentiva 25 mg

Trimipramine Zentiva 25 mg is a medicine authorised by Swissmedic under authorisation number 58345. The authorisation holder is Helvepharm 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 19 October 2007 and the authorisation is valid without a time limit. ATC code N06AA06 places the medicine in the group Psychoanaleptics.

  • Dispensing category B
  • Authorisation number 58345
  • ATC N06AA06
  • Synthetic medicines
Authorisation data
Authorisation number58345
NameTrimipramine Zentiva 25 mg
Full nameTrimipramine Zentiva 25 mg, Tabletten
Authorisation holderHelvepharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeN06AA06
First authorisation19 October 2007
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Trimipramine Zentiva 25 mg, TablettenB19 October 2007
2Trimipramine Zentiva 100 mg, TablettenB19 October 2007

Scroll the table sideways

Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
950Tablette(n)N06AA0601.06.0.B
10200 (4 x 50)Tablette(n)N06AA0601.06.0.B
1120Tablette(n)N06AA0601.06.0.B
12100Tablette(n)N06AA0601.06.0.B

Scroll the table sideways

Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Trimipramine Zentiva 25 mg authorised in Switzerland?

Yes. Trimipramine Zentiva 25 mg is authorised by Swissmedic under authorisation number 58345, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Trimipramine Zentiva 25 mg have?

Trimipramine Zentiva 25 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 Trimipramine Zentiva 25 mg?

The authorisation holder is Helvepharm 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.

Authorisation in Switzerland?

About 2 minutes. No obligation.

First, a little about your business.

Your answers stay in this page until you send your enquiry.

What would you like to achieve?

Your project

Where can we reach you?

You can go back to review your answers before sending.

* Required fields
Prefer email? info@swissmedicinesdirectory.com