Veterinary Medicines

Leventa 1 mg/ml oral solution for dogs

Authorised
  • Levothyroxine sodium
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Product identification

Medicine name:
Leventa 1 mg/ml oral solution for dogs
Leventa 1 mg/ml oral solution for dogs
Active substance:
  • Levothyroxine sodium
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Levothyroxine sodium
    1.00
    milligram(s)
    /
    1.00
    millilitre(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:
  • Valid
Authorised in:
  • Ireland
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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet Productions
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/199/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0182/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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