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.

Ashexol 350 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Ashexol 350

Approved

STANDARD

Ashexol 350

Auskorea Pharm Co., Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 0ee6ec7c6eeb85ca
Company: Auskorea Pharm Co., Ltd.
Type: Standard

Approval Details

Approval Id: 0ee6ec7c6eeb85ca
Drug Approval Philippines Name: Ashexol 350
Product Name: Ashexol 350
Registration Number: DRP-9640
Brand Name: Ashexol 350
Generic Name: Iodine (as Iohexol)
Dosage Form: Solution For Injection
Dosage Strength: 350 mg/mL (equivalent to 755 mg/mL lohexol)
Manufacturer: Auskorea Pharm Co., Ltd.
Importer: JLT Pharma, Inc.
Distributor: JLT Pharma, Inc.
Issuance Date: 26 April 2021
Expiry Date: 26 April 2026
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

0ee6ec7c6eeb85ca

Type

Standard

Back to Philippines FDA Approvals