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DOBURIS - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/DOBURIS

Approved

STANDARD

DOBURIS

Troikaa Pharmaceuticals Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 95a724ee550f81be
Company: Troikaa Pharmaceuticals Ltd.
Type: Standard

Approval Details

Approval Id: 95a724ee550f81be
Drug Approval Philippines Name: DOBURIS
Product Name: DOBURIS
Registration Number: DR-XY46922
Brand Name: DOBURIS
Generic Name: Dobutamine Hydrochloiride
Dosage Form: Solution For Intravenous Infusion
Dosage Strength: 50 mg/ mL
Manufacturer: Troikaa Pharmaceuticals Ltd.
Importer: Troikaa Pharmaceuticals Philippines, Inc.
Distributor: Troikaa Pharmaceuticals Philippines, Inc.
Company Detail Path: /organization/a1bbfc20fa5a1fdf/troikaa-pharmaceuticals-ltd
Issuance Date: 31 October 2020
Expiry Date: 31 October 2025
Pharmacologic Category: Cardiac Stimulant (Adrenergic and dopaminergic agent)
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

95a724ee550f81be

Type

Standard

Back to Philippines FDA Approvals