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HSA Approval

IMOVANE TABLET 7.5 mg

SIN05047P

IMOVANE TABLET 7.5 mg

IMOVANE TABLET 7.5 mg

May 26, 1988

SANOFI-AVENTIS SINGAPORE PTE. LTD.

SANOFI-AVENTIS SINGAPORE PTE. LTD.

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantSANOFI-AVENTIS SINGAPORE PTE. LTD.
Licence HolderSANOFI-AVENTIS SINGAPORE PTE. LTD.

Product Classification

D
Drug Type
Therapeutic
F
Forensic Class
Prescription Only
HSA Singapore Classification

Formulation Information

TABLET, FILM COATED

**Dosage and method of administration** Use the lowest effective dose. IMOVANE should be taken in a single intake and not be re-administered during the same night. Adults: the recommended dose is one 7.5 mg IMOVANE tablet by oral route. This dose should not be exceeded. As with all hypnotics, long-term use of zopiclone is not recommended. Treatment should be as short as possible and should not exceed four weeks including the period of tapering off. Extension beyond the maximum treatment period should not take place without re-evaluation of the patient's status, since the risk of abuse and dependence increases with the duration of treatment. The product must be taken just before retiring for the night. **Treatment duration** Treatment should be as short as possible and should not exceed four weeks including the period of tapering off. Extension beyond the maximum treatment period should not take place without re-evaluation of the patient's status. **Special populations** In elderly and in patients with impaired liver function or chronic respiratory insufficiency: a starting dose of 3.75 mg zopiclone (half a tablet) is recommended initially. The dosage subsequently may be increased to 7.5 mg. In patients with renal insufficiency: although no accumulation of zopiclone or of its metabolites has been detected in cases of renal insufficiency, it is recommended that patients with impaired renal function should start treatment with 3.75 mg. The safe and effective dose of zopiclone has not been established in children and young adults less than 18 years.

ORAL

Medical Information

**Therapeutic indications** IMOVANE is intended for treatment of short-term treatment of insomnia in adults (including difficulties with falling asleep, nocturnal awakening, and early wakening). How should this medicinal product be used _Strictly follow the recommended dosage unless directed otherwise by the physician._

**Contraindications** IMOVANE is contraindicated in patients: - With myasthenia gravis - With hypersensitivity to zopiclone or any of the excipients - With respiratory failure - With severe sleep apnea syndrome - With severe hepatic insufficiency - Who have previously experienced complex sleep behaviors after taking IMOVANE

N05CF01

zopiclone

Manufacturer Information

SANOFI-AVENTIS SINGAPORE PTE. LTD.

Opella Healthcare International SAS

Active Ingredients

ZOPICLONE

7.5 mg

Zopiclone

Documents

Package Inserts

Imovane 7.5mg PI.pdf

Approved: October 4, 2022

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IMOVANE TABLET 7.5 mg - HSA Approval | MedPath