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.

Nuphos-500 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Nuphos-500

Approved

STANDARD

Nuphos-500

Zee Laboratories🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: c5a0312c4f556efe
Company: Zee Laboratories
Type: Standard

Approval Details

Approval Id: c5a0312c4f556efe
Drug Approval Philippines Name: Nuphos-500
Product Name: Nuphos-500
Registration Number: DR-XY42517
Brand Name: Nuphos-500
Generic Name: Cylophosphamide
Dosage Form: Powder For Iv Injection
Dosage Strength: 500 mg
Manufacturer: Zee Laboratories
Importer: Eon Pharmatek Inc.
Distributor: Eon Pharmatek Inc.
Issuance Date: 26 July 2023
Expiry Date: 02 September 2028
Pharmacologic Category: ANTINEOPLASTIC
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

c5a0312c4f556efe

Type

Standard

Back to Philippines FDA Approvals