Skip to main content

MedPath Trial Home

Organizations News Research

Data Sources:ClinicalTrials.govEU CTRFDAEMANMPATGAHealth CanadaWHO ICTRP

MedPath Trial Home

Search trials. Track pipelines. Understand approvals. With AI-powered intelligence for clinical research.

Product

Clinical Trials
Drug Intelligence
Global Approvals
AI Research
Pricing

Resources

FAQ
Search

Company

News
About
Contact

Legal

Privacy Policy
Terms of Service

Disclaimer: This website provides information retrieval and data analysis services. The content does not constitute medical advice. Eligibility assessments are for reference only and should not replace consultation with qualified healthcare professionals. Data is sourced from public registries and regulatory agencies; MedPath does not guarantee completeness or accuracy. Always verify information with primary sources.

© 2026 MedPath Trial. All rights reserved.

We value your privacy

We use cookies to analyze site traffic and improve your experience. See our Privacy Policy.

Approvals/Philippines FDA/Ketosenz

Approved

STANDARD

Ketosenz

Myungmoon Pharmaceuticals Co., Ltd🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: e9356eaa204e9197
Company: Myungmoon Pharmaceuticals Co., Ltd
Type: Standard

Approval Details

Approval Id: e9356eaa204e9197
Drug Approval Philippines Name: Ketosenz
Product Name: Ketosenz
Registration Number: DRP-2382-12
Brand Name: Ketosenz
Generic Name: Ketorolac trometamol
Dosage Form: Solution For Injection (Im/Iv)
Dosage Strength: 30mg/mL
Manufacturer: Myungmoon Pharmaceuticals Co., Ltd
Importer: H & B Pharma International Inc
Distributor: Marcburg Philippines, Inc.
Issuance Date: 24 January 2025
Expiry Date: 12 April 2030
Pharmacologic Category: Non-Opioid Analgesic
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

e9356eaa204e9197

Type

Standard

Back to Philippines FDA Approvals

Ketosenz - Philippines FDA Drug Approval Details