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Ibusoft 200 - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Ibusoft 200
Approved
STANDARD
Ibusoft 200
Humanwell Puracap Pharmaceutical (Wuhan) Co. Ltd
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
25a8f7fc50636af1
Company
Humanwell Puracap Pharmaceutical (Wuhan) Co. Ltd
Type
Standard
Approval Details
Approval Id
25a8f7fc50636af1
Drug Approval Philippines Name
Ibusoft 200
Product Name
Ibusoft 200
Registration Number
DRP-9952
Brand Name
Ibusoft 200
Generic Name
Ibuprofen
Dosage Form
Softgel Capsule
Dosage Strength
200mg
Manufacturer
Humanwell Puracap Pharmaceutical (Wuhan) Co. Ltd
Importer
AMB HK Enterprises Inc.
Distributor
AMB HK Enterprises Inc.
Issuance Date
27 April 2025
Expiry Date
13 April 2031
Pharmacologic Category
Non-Steroidal Anti-Inflammatory Drug (NSAID)/Analgesic/Antipyretics
Classification
Over-the-Counter (OTC) Drug
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
25a8f7fc50636af1
Type
Standard
Back to Philippines FDA Approvals