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/Coxzel

Approved

STANDARD

Coxzel

Stallion Laboratories Pvt. Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 5cb634049728ef8c
Company: Stallion Laboratories Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: 5cb634049728ef8c
Drug Approval Philippines Name: Coxzel
Product Name: Coxzel
Registration Number: DRP-2828-02
Brand Name: Coxzel
Generic Name: Celecoxib
Dosage Form: Capsule
Dosage Strength: 200 mg
Manufacturer: Stallion Laboratories Pvt. Ltd.
Importer: Suhitas Pharmaceuticals Inc.
Distributor: Starpharm, Inc.
Issuance Date: 24 November 2020
Expiry Date: 12 December 2025
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

5cb634049728ef8c

Type

Standard

Back to Philippines FDA Approvals

Coxzel - Philippines FDA Drug Approval Details