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Mucunxt - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Mucunxt

Approved

STANDARD

Mucunxt

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

Approval Date: Jul 14, 2025
Approval ID: 4e5160b7546ea77a
Company: Azarias Pharmaceutical Laboratories Inc.,
Type: Standard

Approval Details

Approval Id: 4e5160b7546ea77a
Drug Approval Philippines Name: Mucunxt
Product Name: Mucunxt
Registration Number: DRP-14227
Brand Name: Mucunxt
Generic Name: Guaifenesin + Phenylpropanolamine Hydrochloride + Chlorphenamine Maleate
Dosage Form: Syrup
Dosage Strength: 100 mg/ 6.5 mg/ 2 mg per 5mL
Manufacturer: Azarias Pharmaceutical Laboratories Inc.,
Trader: St. Raphael Archangel Pharmaceutical Product Distribution
Issuance Date: 31 July 2023
Expiry Date: 31 July 2028
Classification: Over-the-Counter (OTC) Drug

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

4e5160b7546ea77a

Type

Standard

Back to Philippines FDA Approvals