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/Piperax

Approved

STANDARD

Piperax

Affy Parenterals🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 7cd2ef99228d8554
Company: Affy Parenterals
Type: Standard

Approval Details

Approval Id: 7cd2ef99228d8554
Drug Approval Philippines Name: Piperax
Product Name: Piperax
Registration Number: DRP-7694
Brand Name: Piperax
Generic Name: Piperacillin (As Sodium) + Tazobactam (As Sodium)
Dosage Form: Powder For Solution For Injection
Dosage Strength: 4 g/ 500 mg
Manufacturer: Affy Parenterals
Trader: Austere Pharmaceuticals
Importer: Biocare Lifesciences Inc.
Distributor: Biocare Lifesciences Inc.
Issuance Date: 28 March 2022
Expiry Date: 27 March 2027
Pharmacologic Category: ANTIBACTERIAL (PENICILLINS)
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

7cd2ef99228d8554

Type

Standard

Back to Philippines FDA Approvals

Piperax - Philippines FDA Drug Approval Details