DIGESTIA SUSPENSION ORAL PARA TERNEROS LACTANTES, LECHONES LACTANTES, CORDEROS LACTANTES, CABRITOS LACTANTES Y CACHORROS LACTANTES
DIGESTIA SUSPENSION ORAL PARA TERNEROS LACTANTES, LECHONES LACTANTES, CORDEROS LACTANTES, CABRITOS LACTANTES Y CACHORROS LACTANTES
Authorised
- Calcium hydrogen phosphate (anhydrous)
- Magnesium sulfate heptahydrate
- Calcium chloride dihydrate
- Potassium chloride
- Sodium chloride
- Hydrochloric acid
- Dimeticone
- PEPSIN
Product identification
Medicine name:
DIGESTIA SUSPENSION ORAL PARA TERNEROS LACTANTES, LECHONES LACTANTES, CORDEROS LACTANTES, CABRITOS LACTANTES Y CACHORROS LACTANTES
Active substance:
- Calcium hydrogen phosphate (anhydrous)
- Magnesium sulfate heptahydrate
- Calcium chloride dihydrate
- Potassium chloride
- Sodium chloride
- Hydrochloric acid
- Dimeticone
- PEPSIN
Target species:
-
Cattle (calf)
-
Sheep (lamb)
-
Pig (piglet)
-
Dog (puppy)
-
Goat (kid)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Calcium hydrogen phosphate (anhydrous)2.50milligram(s)1.00millilitre(s)
-
Magnesium sulfate heptahydrate2.50milligram(s)1.00millilitre(s)
-
Calcium chloride dihydrate0.05milligram(s)1.00millilitre(s)
-
Potassium chloride0.70milligram(s)1.00millilitre(s)
-
Sodium chloride2.50milligram(s)1.00millilitre(s)
-
Hydrochloric acid16.76milligram(s)1.00millilitre(s)
-
Dimeticone26.40milligram(s)1.00millilitre(s)
-
PEPSIN6.70milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle (calf)
-
Meat and offal0day
-
-
Sheep (lamb)
-
Meat and offal0day
-
-
Pig (piglet)
-
Meat and offal0day
-
-
Dog (puppy)
-
Meat and offal0day
-
-
Goat (kid)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA09AC01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Available in:
-
Spain
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- CZ Vaccines S.A.U.
Marketing authorisation date:
Manufacturing sites for batch release:
- CZ Vaccines S.A.U.
Responsible authority:
- Spanish Agency For Medicines And Medical Devices
Authorisation number:
- 2936 ESP
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
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 3/10/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 3/10/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 3/10/2024
How useful was this page?: