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.

Crolameen - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Crolameen

Approved

STANDARD

Crolameen

La Croesus Pharma, Inc.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 74ee8a1d4a1b3ca6
Company: La Croesus Pharma, Inc.
Type: Standard

Approval Details

Approval Id: 74ee8a1d4a1b3ca6
Drug Approval Philippines Name: Crolameen
Product Name: Crolameen
Registration Number: DR-XY30219
Brand Name: Crolameen
Generic Name: Phenylpropanolamine Hydrochloride
Dosage Form: Syrup
Dosage Strength: 12.5mg/5mL
Manufacturer: La Croesus Pharma, Inc.
Distributor: Medilyn Drug
Issuance Date: 27 February 2024
Expiry Date: 19 February 2029
Pharmacologic Category: Nasal Decongestant
Classification: Over-the-Counter (OTC)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

74ee8a1d4a1b3ca6

Type

Standard

Back to Philippines FDA Approvals