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DELEXARD - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/DELEXARD

Approved

STANDARD

DELEXARD

PT Ferron Par Pharmaceuticals🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 4c8883fbb8e86e64
Company: PT Ferron Par Pharmaceuticals
Type: Standard

Approval Details

Approval Id: 4c8883fbb8e86e64
Drug Approval Philippines Name: DELEXARD
Product Name: DELEXARD
Registration Number: DRP-8132-01
Brand Name: DELEXARD
Generic Name: DOBUTAMINE (as hydrochloride)
Dosage Form: Solution For IV Injection
Dosage Strength: 50 mg/mL (250 mg/5 mL)
Manufacturer: PT Ferron Par Pharmaceuticals
Trader: PT. Dexa Medica
Importer: Glorious Dexa Mandaya, Inc.
Distributor: Delex Pharma International, Inc.
Issuance Date: 31 May 2024
Expiry Date: 28 April 2029
Pharmacologic Category: Adrenergic Agent
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

4c8883fbb8e86e64

Type

Standard

Back to Philippines FDA Approvals