Decivac FMD DOE
Decivac FMD DOE
Authorised
- Foot-and-mouth disease virus, serotype A, Inactivated
- Foot-and-mouth disease virus, serotype O, Inactivated
- Foot-and-mouth disease virus, serotype C, Inactivated
- Foot-and-mouth disease virus, serotype Asia 1, Inactivated
- Foot-and-mouth disease virus, serotype SAT 1, Inactivated
- Foot-and-mouth disease virus, serotype SAT 2, Inactivated
Product identification
Medicine name:
Decivac FMD DOE
Active substance:
- Foot-and-mouth disease virus, serotype A, Inactivated
- Foot-and-mouth disease virus, serotype O, Inactivated
- Foot-and-mouth disease virus, serotype C, Inactivated
- Foot-and-mouth disease virus, serotype Asia 1, Inactivated
- Foot-and-mouth disease virus, serotype SAT 1, Inactivated
- Foot-and-mouth disease virus, serotype SAT 2, Inactivated
Target species:
-
Sheep
-
Cattle
-
Goat
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Foot-and-mouth disease virus, serotype A, Inactivated3.00/50% Protective Dose1.00Dose
-
Foot-and-mouth disease virus, serotype O, Inactivated3.00/50% Protective Dose1.00Dose
-
Foot-and-mouth disease virus, serotype C, Inactivated3.00/50% Protective Dose1.00Dose
-
Foot-and-mouth disease virus, serotype Asia 1, Inactivated3.00/50% Protective Dose1.00Dose
-
Foot-and-mouth disease virus, serotype SAT 1, Inactivated3.00/50% Protective Dose1.00Dose
-
Foot-and-mouth disease virus, serotype SAT 2, Inactivated3.00/50% Protective Dose1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- BFAV/MKS/2/2000
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
German (PDF)
Published on: 29/03/2022