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Seafurox 1500 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Seafurox 1500

Approved

STANDARD

Seafurox 1500

Yeluri Formulations Pvt. Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: b58bab3ae8ed0046
Company: Yeluri Formulations Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: b58bab3ae8ed0046
Drug Approval Philippines Name: Seafurox 1500
Product Name: Seafurox 1500
Registration Number: DRP-11572
Brand Name: Seafurox 1500
Generic Name: Cefuroxime (as sodium)
Dosage Form: Powder for Injection (IM/IV)
Dosage Strength: 1.5 g
Manufacturer: Yeluri Formulations Pvt. Ltd.
Importer: Seapharma International, Inc.
Distributor: Seapharma International, Inc.
Issuance Date: 31 March 2022
Expiry Date: 31 March 2027
Pharmacologic Category: Second Generation Cephalosporin
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

b58bab3ae8ed0046

Type

Standard

Back to Philippines FDA Approvals