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HSA Approval

YUPELRI® INHALATION SOLUTION 175MCG/3ML

SIN16336P

YUPELRI® INHALATION SOLUTION 175MCG/3ML

YUPELRI® INHALATION SOLUTION 175MCG/3ML

September 28, 2021

MYLAN PHARMACEUTICALS PTE. LTD.

MYLAN PHARMACEUTICALS PTE. LTD.

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantMYLAN PHARMACEUTICALS PTE. LTD.
Licence HolderMYLAN PHARMACEUTICALS PTE. LTD.

Product Classification

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

Formulation Information

SOLUTION

**2 DOSAGE AND ADMINISTRATION** The recommended dose of YUPELRI inhalation solution is one 175 mcg unit-dose vial administered once daily by nebulizer using a mouthpiece. YUPELRI should be administered by the orally inhaled route via a standard jet nebulizer connected to an air compressor (See Patient Information – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). The safety and efficacy of YUPELRI have been established in clinical trials when administered using the PARI LC® Sprint nebulizer with a mouthpiece and the PARI Trek® S compressor. The safety and efficacy of YUPELRI delivered from non-compressor-based nebulizer systems have not been established. The YUPELRI unit-dose vial should only be removed from the foil pouch and opened IMMEDIATELY BEFORE USE. The vial and any residual content should be discarded after use. No dosage adjustment is required for geriatric patients, or patients with renal impairment _\[see sections 8.5, 8.7, Clinical Pharmacology (12.3)_ – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_ _\]_. The drug compatibility (physical and chemical), efficacy, and safety of YUPELRI when mixed with other drugs in a nebulizer have not been established.

RESPIRATORY (INHALATION)

Medical Information

**1 INDICATIONS AND USAGE** YUPELRI inhalation solution is indicated for the maintenance treatment of patients with chronic obstructive pulmonary disease (COPD).

**4 CONTRAINDICATIONS** YUPELRI is contraindicated in patients with hypersensitivity to revefenacin or any component of this product.

R03BB08

revefenacin

Manufacturer Information

mylan pharmaceuticals pte. ltd.

The Ritedose Corporation (TRC)

Active Ingredients

Revefenacin

175 mcg /3 ml

Revefenacin

Documents

Package Inserts

Yupelri inhalation solution PI.pdf

Approved: September 28, 2021

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