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.

Jingro - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Jingro

Approved

STANDARD

Jingro

Eurolife Healthcare Pvt. Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 57d4174a25a845f8
Company: Eurolife Healthcare Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: 57d4174a25a845f8
Drug Approval Philippines Name: Jingro
Product Name: Jingro
Registration Number: DRP-16556
Brand Name: Jingro
Generic Name: Ciprofloxacin
Dosage Form: Solution for IV Infusion
Dosage Strength: 2 mg/mL (200 mg/ 100 mL)
Manufacturer: Eurolife Healthcare Pvt. Ltd.
Importer: Aglobal Care, Inc.
Distributor: Aglobal Care, Inc.
Issuance Date: 28 April 2025
Expiry Date: 28 April 2030
Pharmacologic Category: Antibacterial (Fluoroquinolone)
Classification: Prescription (Rx) Drug

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

57d4174a25a845f8

Type

Standard

Back to Philippines FDA Approvals