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Bupron XL 150 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Bupron XL 150

Approved

STANDARD

Bupron XL 150

Sun Pharmaceuticals Industries Limited🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: ec7e68f135ef0a2e
Company: Sun Pharmaceuticals Industries Limited
Type: Standard

Approval Details

Approval Id: ec7e68f135ef0a2e
Drug Approval Philippines Name: Bupron XL 150
Product Name: Bupron XL 150
Registration Number: DR-XY48312
Brand Name: Bupron XL 150
Generic Name: Bupropion Hydrochloride
Dosage Form: Extended Release Tablet
Dosage Strength: 150 mg
Manufacturer: Sun Pharmaceuticals Industries Limited
Importer: Sun Pharma Philippines, Inc.
Distributor: Sun Pharma Philippines, Inc.
Issuance Date: 31 July 2024
Expiry Date: 25 August 2027
Pharmacologic Category: Anti-depressant
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

ec7e68f135ef0a2e

Type

Standard

Back to Philippines FDA Approvals