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IOBET - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/IOBET

Approved

STANDARD

IOBET

FDC LIMITED🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: c5a17dd1d816eda1
Company: FDC LIMITED
Type: Standard

Approval Details

Approval Id: c5a17dd1d816eda1
Drug Approval Philippines Name: IOBET
Product Name: IOBET
Registration Number: DRP-5295
Brand Name: IOBET
Generic Name: BETAXOLOL (AS HYDROCHLORIDE)
Dosage Form: Ophthalmic Solution (Eye Drops)
Dosage Strength: 5 mg/mL (0.5w/v)
Manufacturer: FDC LIMITED
Importer: Penta Labs Australia Philippines
Distributor: Penta Labs Australia Philippines
Company Detail Path: /organization/61863ac51cf73658/fdc-limited
Issuance Date: 31 May 2024
Expiry Date: 15 May 2029
Pharmacologic Category: Antiglaucoma
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

c5a17dd1d816eda1

Type

Standard

Back to Philippines FDA Approvals