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HSA Approval

PERAZODIN 75 TABLET 75 mg

SIN00470P

PERAZODIN 75 TABLET 75 mg

PERAZODIN 75 TABLET 75 mg

April 27, 1988

GOLDPLUS UNIVERSAL PTE LTD

GOLDPLUS UNIVERSAL PTE LTD

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantGOLDPLUS UNIVERSAL PTE LTD
Licence HolderGOLDPLUS UNIVERSAL PTE LTD

Product Classification

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

Formulation Information

TABLET, SUGAR COATED

**Dosage and method of administration** Dosage _Adults_ 300–600 mg daily in three or four divided doses. _Children_ Perazodin is not recommended for children. Method of administration Oral administration. Perazodin should usually be taken before meals.

ORAL

Medical Information

**Indications** An adjunct to oral anti-coagulation for prophylaxis of thrombo-embolism associated with prosthetic heart valves.

**Contraindications** Hypersensitivity to the active substance(s) or to any of the excipients listed in section List of excipients – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_. In case of rare hereditary conditions that may be incompatible with an excipient of the product (please refer to section Warnings and Precautions – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_) the use of the product is contraindicated.

B01AC07

dipyridamole

Manufacturer Information

GOLDPLUS UNIVERSAL PTE LTD

REMEDICA LTD

Active Ingredients

DIPYRIDAMOLE

75 mg

Dipyridamole

Documents

Package Inserts

Perazodin Tablet PI.pdf

Approved: December 21, 2022

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PERAZODIN 75 TABLET 75 mg - HSA Approval | MedPath