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HSA Approval

AA-AMILZIDE TABLET

Approval Number

SIN06538P

Drug Name

AA-AMILZIDE TABLET

Product Name

AA-AMILZIDE TABLET

Approval Date

August 22, 1991

Registrant

PHARMAFORTE SINGAPORE PTE LTD

Licence Holder

PHARMAFORTE SINGAPORE PTE LTD

Regulatory Information

Registrant

PHARMAFORTE SINGAPORE PTE LTD

Licence Holder

PHARMAFORTE SINGAPORE PTE LTD

Drug Type

Therapeutic

Forensic Classification

Prescription Only

Formulation Information

Dosage Form

TABLET

Route of Administration

ORAL

Medical Information

ATC Code

C03EA01

ATC Item Name

hydrochlorothiazide and potassium-sparing agents

Manufacturer Information

Pharmaceutical Manufacturer

PHARMAFORTE SINGAPORE PTE LTD

Manufacturers

APOTEX INC

Active Ingredients

Ingredient Name

AMILORIDE HCl

Strength

5 mg

Drug MonographAmiloride

Ingredient Name

HYDROCHLOROTHIAZIDE

Strength

50 mg

Drug MonographHydrochlorothiazide

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