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Fentare - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Fentare

Approved

STANDARD

Fentare

Yichang Humanwell Pharmaceutical Co., Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: a3d887354780f633
Company: Yichang Humanwell Pharmaceutical Co., Ltd.
Type: Standard

Approval Details

Approval Id: a3d887354780f633
Drug Approval Philippines Name: Fentare
Product Name: Fentare
Registration Number: DRP-15138
Brand Name: Fentare
Generic Name: Remifentanil (as hydrochloride)
Dosage Form: Lyophilized Powder for Injection (I.V.)
Dosage Strength: 1 mg
Manufacturer: Yichang Humanwell Pharmaceutical Co., Ltd.
Importer: Philcare Pharma, Inc.
Distributor: Philcare Pharma, Inc.
Company Detail Path: /organization/yichang-humanwell-pharmaceutical-co-ltd
Issuance Date: 10 May 2024
Expiry Date: 10 May 2029
Pharmacologic Category: Opioid Anesthetic
Classification: Prescription (Rx) Drug

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

a3d887354780f633

Type

Standard

Back to Philippines FDA Approvals