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.

Vanclaire - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Vanclaire

Approved

STANDARD

Vanclaire

Venus Remedies, Limited🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 576ab6313d09476c
Company: Venus Remedies, Limited
Type: Standard

Approval Details

Approval Id: 576ab6313d09476c
Drug Approval Philippines Name: Vanclaire
Product Name: Vanclaire
Registration Number: DRP-10631-03
Brand Name: Vanclaire
Generic Name: Vancomycin (as hydrochloride)
Dosage Form: Powder for Injection (IV)
Dosage Strength: 1 g
Manufacturer: Venus Remedies, Limited
Importer: Afree Pharmaceutical Distribution Corp.
Distributor: Jackson Pharmaceuticals Inc
Issuance Date: 24 October 2022
Expiry Date: 10 November 2026
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

576ab6313d09476c

Type

Standard

Back to Philippines FDA Approvals