LUTRELEF subst sèche 3.2 mg c solv flac

7680473660388 CH-47366 H01CA01 07.03.1.

Reimbursement limitations:

LUTRELEF

Hypogonadisme hypothalamo-hypophysaire chez l'homme.
Activation de la fonction ovarienne chez la femme en cas de:

LUTRELEF subst sèche 3.2 mg c solv flac
LUTRELEF subst sèche 3.2 mg c solv flac
LUTRELEF subst sèche 3.2 mg c solv flac
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Details

Product number
4736602
CPT
-
Packaging group
1
Unit
Durchstechflasche(n)
Composition
Praeparatio cryodesiccata: gonadorelini acetas 3.2 mg corresp. gonadorelinum 2.91 mg, mannitolum acidum hydrochloridum, pro vitro. Solvens: natrii chloridum corresp. natrium 35.4 mg, acidum hydrochloridum, aqua ad iniectabile 10 ml.

Articles (1)

Lutrelef 3,2 mg, Injektionspräparat
Injektionspräparat
1
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Professional SmPC
Allemand
28/07/2022
Professional SmPC
Français
28/07/2022
Professional SmPC
Italien
28/07/2022

Detailed composition

Substance Quantity Type Category
SOLV
- Substance HNIDK
PRC
3.2 MG Substance WIZUS
SOLV
35.4 MG Substance HBESI
PRC
2.91 MG Substance Wirkstoff (Principe actif)
SOLV
- Substance HNIDK
PRC
- Substance HNIDK
PRC
- Substance HNIDK
SOLV
10.0 ML Substance HNIDK

Reimbursement information

Public price
CHF 343.45
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 15/03/1991

Authorization holder

Ferring AG

6340 Baar

Authorization information

Swissmedic authorization number
47366
Drug name
Lutrelef, Injektionspräparat
Galenic form
PULMJ
ATC Code
H01CA01
Authorization status
Z
Dispensation category
B
First authorization
04/08/1986
Authorization expiration date
31/12/9999
IT number
07.03.1.
Domain
Human medicine
Field of application
Hypothalamische Amenorrhoe, zentraler Hypogonadismus beim Mann

Packaging details

Description (FR)
LUTRELEF subst sèche 3.2 mg c solv flac
Description (DE)
LUTRELEF Trockensub 3.2 mg c Solv Durchstf
Market launch
04/08/1986
Narcotic (BTM)
No

Other packaging sizes