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.

Flevoxcin Iv - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Flevoxcin Iv

Approved

STANDARD

Flevoxcin Iv

Akums Drugs & Pharmaceutical Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 951feb773e6083be
Company: Akums Drugs & Pharmaceutical Ltd.
Type: Standard

Approval Details

Approval Id: 951feb773e6083be
Drug Approval Philippines Name: Flevoxcin Iv
Product Name: Flevoxcin Iv
Registration Number: DRP-3937-03
Brand Name: Flevoxcin Iv
Generic Name: Levofloxacin (As Hemihydrate)
Dosage Form: Solution for Intravenous Infusion
Dosage Strength: 5 mg/mL (500mg/100mL)
Manufacturer: Akums Drugs & Pharmaceutical Ltd.
Importer: ambica international corp.
Distributor: gx international, inc.
Issuance Date: 27 May 2022
Expiry Date: 04 September 2027
Pharmacologic Category: Antibacterial (Quinolone)
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

951feb773e6083be

Type

Standard

Back to Philippines FDA Approvals