Elisaviatris 2 mg - 0.035 mg coat. tabl.

Pays: Belgique

Langue: anglais

Source: AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

Achète-le

Ingrédients actifs:

Ethinylestradiol 0,035 mg; Cyproterone acetate 2 mg

Disponible depuis:

Viatris GX BV-SRL

Code ATC:

G03HB01

DCI (Dénomination commune internationale):

Cyproterone acetate; Ethinylestradiol

Dosage:

2 mg - 0,035 mg

forme pharmaceutique:

Coated tablet

Composition:

Cyproterone acetate 2 mg; Ethinylestradiol 35 µg

Mode d'administration:

Oral use

Domaine thérapeutique:

Cyproterone and Estrogen

Descriptif du produit:

CTI code: 239181-09 - Pack size: 9 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-07 - Pack size: 7 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-08 - Pack size: 8 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-05 - Pack size: 5 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-06 - Pack size: 6 x 21 - Commercialisation status: YES - FMD code: 05099151910639 - CNK code: 2216208 - Delivery mode: Medical prescription; CTI code: 239181-03 - Pack size: 3 x 21 - Commercialisation status: YES - FMD code: 05099151910646 - CNK code: 2095404 - Delivery mode: Medical prescription; CTI code: 239181-04 - Pack size: 4 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-01 - Pack size: 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-12 - Pack size: 12 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-02 - Pack size: 2 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-10 - Pack size: 10 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription; CTI code: 239181-11 - Pack size: 11 x 21 - Commercialisation status: NO - Delivery mode: Medical prescription

Statut de autorisation:

Commercialised: Yes

Date de l'autorisation:

2002-08-05

Documents dans d'autres langues

Notice patient Notice patient allemand 01-08-2023
MMR MMR allemand 01-07-2022
Notice patient Notice patient français 01-08-2023
DHPC DHPC français 23-02-2023
Notice patient Notice patient néerlandais 01-08-2023
DHPC DHPC néerlandais 23-02-2023