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.

Nexefer - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Nexefer

Approved

STANDARD

Nexefer

Theon Pharmaceuticals Limited🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: f970e5e3d8c312c4
Company: Theon Pharmaceuticals Limited
Type: Standard

Approval Details

Approval Id: f970e5e3d8c312c4
Drug Approval Philippines Name: Nexefer
Product Name: Nexefer
Registration Number: DRP-15886
Brand Name: Nexefer
Generic Name: Cefalexin (as monohydrate)
Dosage Form: Capsule
Dosage Strength: 500 mg
Manufacturer: Theon Pharmaceuticals Limited
Importer: Hexagon Pharmaceuticals Limited
Distributor: Hexagon Pharmaceuticals Limited
Issuance Date: 27 September 2024
Expiry Date: 27 September 2029
Pharmacologic Category: Antibacterial (Cephalosporin)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

f970e5e3d8c312c4

Type

Standard

Back to Philippines FDA Approvals