Gliclazid-Mepha Teva MR 30 mg

Gliclazid-Mepha Teva MR 30 mg is a medicine authorised by Swissmedic under authorisation number 65694. The authorisation holder is Mepha Pharma 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 17 September 2015 and the authorisation is valid without a time limit. ATC code A10BB09 places the medicine in the group Drugs used in diabetes.

  • Dispensing category B
  • Authorisation number 65694
  • ATC A10BB09
  • Synthetic medicines
Authorisation data
Authorisation number65694
NameGliclazid-Mepha Teva MR 30 mg
Full nameGliclazid-Mepha Teva MR 30 mg, Retardtabletten
Authorisation holderMepha Pharma AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeA10BB09
First authorisation17 September 2015
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Gliclazid-Mepha Teva MR 30 mg, RetardtablettenB17 September 2015
2Gliclazid-Mepha Teva MR 60 mg, RetardtablettenB17 September 2015

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
630Tablette(n)A10BB0907.06.2.B
7120Tablette(n)A10BB0907.06.2.B
830Tablette(n)A10BB0907.06.2.B
990Tablette(n)A10BB0907.06.2.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Gliclazid-Mepha Teva MR 30 mg authorised in Switzerland?

Yes. Gliclazid-Mepha Teva MR 30 mg is authorised by Swissmedic under authorisation number 65694, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Gliclazid-Mepha Teva MR 30 mg have?

Gliclazid-Mepha Teva MR 30 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 Gliclazid-Mepha Teva MR 30 mg?

The authorisation holder is Mepha Pharma 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.

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