SAI - Detailed view

KRENOSIN Inj Lös 6 mg/2ml 6 Amp 2 ml

Drug

Name

Krenosin, solution injectable

ATC

C01EB10 - ADENOSINE

02.02.0. – antiarrhythmics

Use

HAM – Human medicine

pharmaceutical form

LSPA – Parenteral solution

Remedy code

S – synthetic products for human use

Dispensing categories

A – Dispensed once only on prescription by a physician or veterinarian (A)

Authorisation status

Z – approved

Authorisation number

51567

Initial registration date

4/6/1992

Expiry date

12/31/9999

Dosage strength

Name

Krenosin, solution injectable

Field of application

Antiarythmique

Dosage strength number

Authorisation status

Z – approved

Package

GTIN**

7680515670139

Trade status*

In trade from / since 4/6/1992

Status

A/R – Authorised / referenced

Package size

6 x 2 mL ampoule(s)

Package code

013

Authorisation status

Z – approved

Declaration

Component

Active substance

6 mg adenosinum

Excipient

natrii chloridum
aqua ad iniectabile

Authorisation holder

GLN**

7601001002340

Address

Sanofi-Aventis (Suisse) SA
route de Montfleury 3
1214 Vernier (GE)

Date of revision of the text

4/29/2025

Information for prof.

Leaflet

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Data source: Swissmedic, *authorisation holder, **Refdata foundation, ***FOPH.