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OCUDOR - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/OCUDOR

Approved

STANDARD

OCUDOR

FDC Limited🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: b64a70619db708ac
Company: FDC Limited
Type: Standard

Approval Details

Approval Id: b64a70619db708ac
Drug Approval Philippines Name: OCUDOR
Product Name: OCUDOR
Registration Number: DRP-5572
Brand Name: OCUDOR
Generic Name: DORZOLAMIDE (as hydrochloride)
Dosage Form: Ophthalmic Solution (Eye Drops)
Dosage Strength: 20 mg/mL
Manufacturer: FDC Limited
Importer: Penta Labs Australia (Philippines)
Distributor: Penta Labs Australia (Philippines)
Company Detail Path: /organization/61863ac51cf73658/fdc-limited
Issuance Date: 31 October 2023
Expiry Date: 06 November 2028
Pharmacologic Category: Carbonic anhydrase inhibitor
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

b64a70619db708ac

Type

Standard

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