Biocom P Vet
Biocom P Vet
Awtorizzat
- Clostridium botulinum, type C, toxoid
- Pseudomonas aeruginosa, serotype 5, strain PA5G-485, Inactivated
- Pseudomonas aeruginosa, serotype 6, strain PA6M-485-JA, Inactivated
- Mink enteritis virus, type 1, strain United, Inactivated
- Pseudomonas aeruginosa, serotype 5, strain PA5M-485-P, Inactivated
- Pseudomonas aeruginosa, serotype 7/8, strain PA7G-485, Inactivated
- Mink enteritis virus, type 2, strain Ithaca, Inactivated
- Pseudomonas aeruginosa, serotype 6, strain PA6G-485, Inactivated
- Pseudomonas aeruginosa, serotype 7, strain PA7M-485-347, Inactivated
- Pseudomonas aeruginosa, serotype 6, strain PA6M-485-JB, Inactivated
Identifikazzjoni tal-prodott
Isem tal-mediċina:
Biocom P Vet
BIOCOM P Vet, injekcinė suspensija audinėms
Metodu ta’ amministrazzjoni:
-
Użu għal taħt il-ġilda
Dettalji tal-prodott
Sustanza attiva / Qawwa:
-
Disponibbli biss fi English40.0080% Protective Dose1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.0080% Protective Dose1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.0080% Protective Dose1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
-
Disponibbli biss fi English1.00relative potency1.00millilitre(s)
Forma farmaċewtika:
-
Suspensjoni għall-injezzjoni
Withdrawal period by route of administration:
-
Użu għal taħt il-ġilda
-
Mink
-
Kodiċi veterinarju anatomiku terapewtiku kimiku (ATCvet):
- QI20CL01
Status tal-awtorizzazzjoni:
-
Valid
Tagħrif addizzjonali
Id-detentur tal-awtorizzazzjoni għat-tqegħid fis-suq:
- United Vaccines Holding B.V.
Marketing authorisation date:
Siti ta’ manifattura b’rilaxx tal-lott:
- Cooperative Federation Of Nobel Animal Keepers Nederasselt U.A.
Awtorità responsabbli:
- State Food And Veterinary Service
Numru tal-awtorizzazzjoni:
- LT/2/17/2424/001-003
Data tal-bidla fl-istatus tal-awtorizzazzjoni:
Numru tal-proċedura:
- NL/V/0227/001
Stati Membri Kkonċernati:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Dokumenti
RV2424.pdf
Lithuanian (PDF)
Niżżel Ippubblikat fuq: 30/05/2022
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