Veterinary medicinal product register

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Data selected by 459 Name doxybactin
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Doxybactin vet 50 mg V/DCP/17/0031 Dechra Regulatory B.V., Nīderlande QJ01AA02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Doxycyclin hyclate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 26-Aug-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0031-01 50 mg 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0031-02 50 mg 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0031-03 50 mg 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0031-04 50 mg 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0031-05 50 mg 10 Kastīte ar blisteri, 10 tablete -
Doxybactin vet 200 mg V/DCP/17/0032 Dechra Regulatory B.V., Nīderlande QJ01AA02 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Doxycyclin hyclate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 26-Aug-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0032-01 200 mg 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0032-02 200 mg 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0032-03 200 mg 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0032-04 200 mg 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0032-05 200 mg 10 Kastīte ar blisteri, 10 tablete -
Doxybactin vet 400 mg V/DCP/17/0033 Dechra Regulatory B.V., Nīderlande QJ01AA02 dogs

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Doxycyclin hyclate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 26-Aug-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0033-01 400 mg 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0033-02 400 mg 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0033-03 400 mg 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0033-04 400 mg 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/17/0033-05 400 mg 10 Kastīte ar blisteri, 10 tablete -
Doxybactin 50 mg V/I/20/0061 Dechra Regulatory B.V., Nīderlande QJ01AA02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Doxycycline
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande;Genera d.d., Horvātija
Date of authorisation/renewal: 24-Nov-2025
Marketing authorisation valid until: 23-Nov-2030
Marketing authorisation procedure: I
Package leaflet: [DOCX] 24112025_LI (24-Nov-2025)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/20/0061-01 50 mg 1 alumīnija/PVC/PE/PVDC blisteris, 10 tablete [PDF]

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