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HSA Approval

Xolair 75mg Powder and Solvent for Solution for Injection

SIN13213P

Xolair 75mg Powder and Solvent for Solution for Injection

Xolair 75mg Powder and Solvent for Solution for Injection

July 7, 2006

NOVARTIS (SINGAPORE) PTE LTD

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantNOVARTIS (SINGAPORE) PTE LTD

Product Classification

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

Formulation Information

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

SUBCUTANEOUS

Medical Information

R03DX05

omalizumab

Manufacturer Information

NOVARTIS (SINGAPORE) PTE LTD

Novartis Pharma Stein AG

Takeda Austria GmbH

DELPHARM DIJON - QUETIGNY

Active Ingredients

Omalizumab

75mg

Omalizumab

Documents

Package Inserts

Xolair PI.pdf

Approved: January 27, 2023

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Xolair 75mg Powder and Solvent for Solution for Injection - HSA Approval | MedPath