HSA Approval

NIFELAT TABLET 10 mg

Approval Number

SIN07228P

Drug Name

Product Name

NIFELAT TABLET 10 mg

Approval Date

October 21, 1992

Registrant

GOLDPLUS UNIVERSAL PTE LTD

Licence Holder

GOLDPLUS UNIVERSAL PTE LTD

Regulatory Information

Registrant

GOLDPLUS UNIVERSAL PTE LTD

Licence Holder

GOLDPLUS UNIVERSAL PTE LTD

Drug Type

Therapeutic

Forensic Classification

Prescription Only

Formulation Information

Dosage Form

TABLET, FILM COATED

Route of Administration

ORAL

Medical Information

ATC Code

C08CA05

ATC Item Name

nifedipine

Manufacturer Information

Pharmaceutical Manufacturer

GOLDPLUS UNIVERSAL PTE LTD

Manufacturers

REMEDICA LTD

Active Ingredients

Ingredient Name

NIFEDIPINE

Strength

10 mg

Drug MonographNifedipine

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NIFELAT TABLET 10 mg

Regulatory Information

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Active Ingredients

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