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Bortether - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Bortether

Approved

STANDARD

Bortether

Therdose Pharma Pvt. Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 4f8c7fbe30d575c1
Company: Therdose Pharma Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: 4f8c7fbe30d575c1
Drug Approval Philippines Name: Bortether
Product Name: Bortether
Registration Number: DRP-5230
Brand Name: Bortether
Generic Name: Bortezomib
Dosage Form: Lyophilized Powder For Injection (I.V)
Dosage Strength: 3.5 mg
Manufacturer: Therdose Pharma Pvt. Ltd.
Importer: MedEthix Incorporated
Distributor: MedEthix Incorporated
Issuance Date: 26 July 2023
Expiry Date: 26 July 2028
Classification: Prescription (RX) Drug

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

4f8c7fbe30d575c1

Type

Standard

Back to Philippines FDA Approvals