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HSA Approval

HEPARINISED SALINE INJECTION 10 iu/ml

SIN12253P

HEPARINISED SALINE INJECTION 10 iu/ml

HEPARINISED SALINE INJECTION 10 iu/ml

April 4, 2003

B. BRAUN SINGAPORE PTE LTD

B. BRAUN SINGAPORE PTE LTD

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantB. BRAUN SINGAPORE PTE LTD
Licence HolderB. BRAUN SINGAPORE PTE LTD

Product Classification

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

Formulation Information

INJECTION

**Dosage and administration** To be determined by the attending physician. For flushing of in-dwelling cannulae, the usual recommended dose is 10 international units to 50 international units every 4 hours.

INTRAVENOUS

Medical Information

**Indications** **Heparinised Saline Injection** is used for flushing of in-dwelling cannulae and maintaining the patency of intravenous injection devices.

**Contraindications** Heparin is contraindicated in patients who are hypersensitive to the drug. It is contraindicated in patients with haemorrhagic diseases; thrombocytopenia and patients who are haemorrhaging or are at risk of haemorrhage including those with haemophilia, subacute bacterial endocarditis, gastric or duodenal ulcer or severe hypertension. It is also contraindicated in patients who have recently undergone surgery at sites where haemorrhage would be an especial risk.

B01AB51

heparin, combinations

Manufacturer Information

B. Braun Singapore Pte Ltd.

B BRAUN MEDICAL INDUSTRIES SDN BHD

Active Ingredients

HEPARIN SODIUM (BOVINE MUCOSA)

10 iu/ml

Heparin

SODIUM CHLORIDE

0.9%

Sodium chloride

Documents

Package Inserts

07 v2_15242561_Heparinised_GIF_A5__SG_150.pdf

Approved: February 7, 2017

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