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HSA Approval

ALU-TAB TABLET 600 mg

SIN02930P

ALU-TAB TABLET 600 mg

ALU-TAB TABLET 600 mg

May 22, 1989

INOVA PHARMACEUTICALS (SINGAPORE) PTE. LIMITED

INOVA PHARMACEUTICALS (SINGAPORE) PTE. LIMITED

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantINOVA PHARMACEUTICALS (SINGAPORE) PTE. LIMITED
Licence HolderINOVA PHARMACEUTICALS (SINGAPORE) PTE. LIMITED

Product Classification

D
Drug Type
Therapeutic
F
Forensic Class
General Sale List
HSA Singapore Classification

Formulation Information

TABLET, FILM COATED

**DOSAGE AND ADMINISTRATION** One to two tablets four times daily or as directed by physician. When used for patients with renal dysfunction the specially formulated film coating allows the whole tablet to be swallowed with a minimum of water.

ORAL

Medical Information

**INDICATIONS** Symptomatic relief of uncomplicated peptic ulcer and gastric hyperacidity. Phosphate binding in renal dysfunction.

**CONTRAINDICATIONS** Hypophosphataemia.

A02AB01

aluminium hydroxide

Manufacturer Information

INOVA PHARMACEUTICALS (SINGAPORE) PTE. LIMITED

Adcock Ingram Limited

Active Ingredients

ALUMINIUM HYDROXIDE (DRIED GEL)

600 mg

Aluminum hydroxide

Documents

Package Inserts

Alu-Tab Tablet 600mg PI.pdf

Approved: May 25, 2009

Download

Patient Information Leaflets

Alu-Tab Tablet PIL.pdf

Approved: July 9, 2014

Download

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ALU-TAB TABLET 600 mg - HSA Approval | MedPath