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HSA Approval

Salofalk Gastro- resistant Prolonged-release Granules 1g/ sachet

SIN14427P

Salofalk Gastro- resistant Prolonged-release Granules 1g/ sachet

Salofalk Gastro- resistant Prolonged-release Granules 1g/ sachet

November 8, 2013

DCH AURIGA SINGAPORE

DCH AURIGA SINGAPORE

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantDCH AURIGA SINGAPORE
Licence HolderDCH AURIGA SINGAPORE

Product Classification

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

Formulation Information

GRANULE, DELAYED RELEASE

**4.2 Posology and method of administration** Posology _Adults and the elderly_ For the treatment of acute episodes of ulcerative colitis Once daily, 1 sachet of Salofalk granules 3g, 1–2 sachets of Salofalk granules 1.5g, 3 sachets of Salofalk granules 1g or 3 sachets of Salofalk granules 500mg (equivalent to 1.5–3.0 g mesalazine daily) preferably to be taken in the morning according to the individual clinical requirement. It is also possible to take the prescribed daily dose in three divided doses (1 sachet of Salofalk granules 500mg 3 times daily or 1 sachet of Salofalk granules 1g 3 times daily) if this is more convenient to the patient. For the maintenance of remission of ulcerative colitis The standard treatment is 0.5 g mesalazine 3 times daily (in the morning, at midday and in the evening) corresponding to a total dose of 1.5 g mesalazine per day. _Paediatric population_ There is only limited documentation for an effect in children (age 6–18 years). Children 6 years of age and older **Active disease:** To be determined individually, starting with 30–50 mg/kg bw/day once daily preferably in the morning or in divided doses. Maximum dose: 75 mg/kg bw/day. The total dose should not exceed the maximum adult dose. **Maintenance treatment:** To be determined individually, starting with 15–30 mg/kg bw/day in divided doses. The total dose should not exceed the recommended adult dose. It is generally recommended that half the adult dose may be given to children up to a body weight of 40 kg and the normal adult dose to those above 40 kg. Method of administration The contents of the sachets of Salofalk granules should not be chewed. The granules should be taken on the tongue and swallowed, without chewing, with plenty of liquid. Both in the treatment of acute inflammatory episodes and during long term treatment, Salofalk granules should be used on a regular basis and consistently in order to achieve the desired therapeutic effects. The duration of use is determined by the physician.

ORAL

Medical Information

**4.1 Therapeutic indications** For the treatment of acute episodes and the maintenance of remission of ulcerative colitis.

**4.3 Contraindications** Salofalk granules are contra-indicated in patients with - hypersensitivity to the active substance, to salicylates or to any of the excipients listed in section 6.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_. - severe impairment of hepatic or renal function.

A07EC02

mesalazine

Manufacturer Information

DCH AURIGA SINGAPORE

Losan Pharma GmbH

Losan Pharma GmbH (Primary packager and Secondary packager)

Active Ingredients

Mesalazine

1000mg/ sachet

Mesalazine

Documents

Package Inserts

Salofalk Gastro-resistant Prolonged-release Granules PI.pdf

Approved: February 18, 2022

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