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Azthrex - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Azthrex

Approved

STANDARD

Azthrex

Azarias Pharmaceutical Laboratories Inc.,🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: c3fafbf0ac45de62
Company: Azarias Pharmaceutical Laboratories Inc.,
Type: Standard

Approval Details

Approval Id: c3fafbf0ac45de62
Drug Approval Philippines Name: Azthrex
Product Name: Azthrex
Registration Number: DRP-3217
Brand Name: Azthrex
Generic Name: Loratadine + Phenylephrine Hydrochloride
Dosage Form: Syrup
Dosage Strength: 5mg/ 5mL
Manufacturer: Azarias Pharmaceutical Laboratories Inc.,
Distributor: STARPHARM INC
Issuance Date: 31 July 2021
Expiry Date: 01 September 2026
Pharmacologic Category: Antihistamine/Nasal Decongestant
Classification: Over-The-Counter (OTC)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

c3fafbf0ac45de62

Type

Standard

Back to Philippines FDA Approvals