Veterinary medicinal product register

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Data selected by 124 Name Thiafeline
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Thiafeline 5 mg V/DCP/13/0024 Le Vet Beheer B.V., Nīderlande QH03BB02 cats

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Thiamazol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lindopharm GmbH, Vācija;Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-Feb-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Apr-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-Apr-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0024-01 5 mg 1 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0024-02 5 mg 2 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0024-03 5 mg 4 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0024-04 5 mg 5 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0024-05 5 mg 10 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
Thiafeline 2.5 mg V/DCP/13/0025 Le Vet Beheer B.V., Nīderlande QH03BB02 cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Thiamazol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lindopharm GmbH, Vācija;Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-Feb-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2019)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-Apr-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0025-01 2,5 mg 1 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0025-02 2,5 mg 2 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0025-03 2,5 mg 4 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0025-04 2,5 mg 5 PVH/Al blisteris (necaurspīdīgs), 30 tablete -
V/DCP/13/0025-05 2,5 mg 10 PVH/Al blisteris (necaurspīdīgs), 30 tablete -

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