MedPath

Azthrex

Brand Name: Azthrex

Generic Name: Loratadine + Phenylephrine Hydrochloride

Active
Registration Number

DRP-3217

Dosage Form

Syrup

Issuance Date

July 31, 2021

Expiry Date

September 1, 2026

Product Information

Philippine FDA product specifications and classification details

Product Specifications

Dosage Strength5mg/ 5mL
PackagingBoston Round, Glass Amber Bottle x 60mL

Classification

C
Classification
Over-The-Counter (OTC)
P
Pharmacologic
Antihistamine/Nasal Decongestant
A
Application
Automatic Renewal
Philippine FDA Classification

Active Ingredients (2)

Complete list of active ingredients in this pharmaceutical product.

LoratadineActive
Monograph: Loratadine
Phenylephrine HydrochlorideActive
Monograph: Phenylephrine

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

Product

Company

Legal

© 2025 MedPath, Inc. All rights reserved.

MedPath - Medical Intelligence Platform