Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Viðurkennt
- Sodium glycerophosphate pentahydrate
- Magnesium chloride hexahydrate
- CALCIUM GLUCONATE FOR INJECTION
Auðkenning lyfsins
Heiti lyfs:
Kaltetan, 250 mg/ml + 80 mg/ml + 10 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan 250 mg/ml + 80 mg/ml + 10 mg/1 ml Roztwór do infuzji
Dýrategundir:
-
Hestur
-
Svín
-
Nautgripir
Íkomuleið:
-
Til notkunar í bláæð
Upplýsingar um lyfið
Lyfjaform:
-
Innrennslislyf, lausn
Withdrawal period by route of administration:
-
Til notkunar í bláæð
- Hestur
-
Mjólk5weekMeat and offal: Zero days. Milk: Zero hours
-
- Svín
-
Kjöt og innmatur5weekMeat and offal: Zero days
-
- Nautgripir
-
Mjólk5weekMeat and offal: Zero days. Milk: Zero hours
-
ATC flokkun (dýralyf):
- QA12AX
Lögformleg staða:
Þessar upplýsingar eru ekki tiltækar fyrir þessa vöru.
Staða markaðsleyfis:
-
Gilt
Authorised in:
-
Pólland
Available in:
-
Pólland
Áletrun:
- Aðeins í boði í English
Viðbótarupplýsingar
Entitlement type:
-
Marketing Authorisation
Markaðsleyfishafi:
- Vet-Agro Multi-Trade Company Sp. z o.o.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
- Multi-Trade Company "Vet-Agro" Sp. z o.o.
Ábyrgt yfirvald:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Markaðsleyfisnúmer:
- 3171
Dagsetning leyfisbreytingar:
Umsjónarland (RMS):
-
Pólland
Númer verkferlis:
- PL/V/0110/001
Þátttökulönd (CMS):
-
Búlgaría
-
Tékkland
-
Grikkland
-
Ungverjaland
-
Ítalía
-
Litáen
-
Portúgal
-
Rúmenía
-
Spánn
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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