Leventa 1 mg/ml oral solution for dogs
Leventa 1 mg/ml oral solution for dogs
Not authorised
- Levothyroxine sodium
Product identification
Medicine name:
Leventa 1 mg/ml oral solution for dogs
Leventa 1 mg/ml oplossing voor oraal gebruik bij honden
Active substance:
- Levothyroxine sodium
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Levothyroxine sodium1.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH03AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Netherlands
Package description:
- 30 mL amber glass bottle with a transparent LDPE insert and with a white HDPE child-resistant cap with tamper-proof closure in a printed carton. A 1 ml oral syringe graduated in 0.05 ml increments is supplied with the product. Pack size: 1 x 30 ml
- 30 mL amber glass bottle with a transparent LDPE insert and with a white HDPE child-resistant cap with tamper-proof closure in a printed carton. A 1 ml oral syringe graduated in 0.05 ml increments is supplied with the product. Pack size: 6 x 30 ml
- 30 mL amber glass bottle with a transparent LDPE insert and with a white HDPE child-resistant cap with tamper-proof closure in a printed carton. A 1 ml oral syringe graduated in 0.05 ml increments is supplied with the product. Pack size: 12 x 30 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Productions S.A.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 10408
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0182/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Dutch (PDF)
Published on: 26/01/2022
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
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