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MoxiDen - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/MoxiDen

Approved

STANDARD

MoxiDen

Makcur Laboratories Ltd🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 0220351722c8c36b
Company: Makcur Laboratories Ltd
Type: Standard

Approval Details

Approval Id: 0220351722c8c36b
Drug Approval Philippines Name: MoxiDen
Product Name: MoxiDen
Registration Number: DRP-11229-01
Brand Name: MoxiDen
Generic Name: Moxifloxacin (as Hydrochloride)
Dosage Form: Ophthalmic Solution
Dosage Strength: 5mg/mL (0.5% w/v)
Manufacturer: Makcur Laboratories Ltd
Importer: Ensight Pharmaceuticals Inc.
Distributor: D&M Pharma Corp.
Issuance Date: 25 May 2022
Expiry Date: 01 April 2027
Pharmacologic Category: Anti-infectives (Fluoroquinolones)
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

0220351722c8c36b

Type

Standard

Back to Philippines FDA Approvals