Dilzem 180 mg RR

Dilzem 180 mg RR is a medicine authorised by Swissmedic under authorisation number 49577. The authorisation holder is Pfizer 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 29 December 1987 and the authorisation is valid without a time limit. ATC code C08DB01 places the medicine in the group Calcium channel blockers.

  • Dispensing category B
  • Authorisation number 49577
  • ATC C08DB01
  • Synthetic medicines
Authorisation data
Authorisation number49577
NameDilzem 180 mg RR
Full nameDilzem 180 mg RR, Retardtabletten
Authorisation holderPfizer AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeC08DB01
First authorisation29 December 1987
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
1Dilzem 180 mg RR, RetardtablettenB29 December 1987

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
2830Tablette(n)C08DB0102.06.1.B
36100Tablette(n)C08DB0102.06.1.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Dilzem 180 mg RR authorised in Switzerland?

Yes. Dilzem 180 mg RR is authorised by Swissmedic under authorisation number 49577, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Dilzem 180 mg RR have?

Dilzem 180 mg RR 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 Dilzem 180 mg RR?

The authorisation holder is Pfizer 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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