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Buderite - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Buderite
Approved
STANDARD
Buderite
Legency Rmedies Pvt. Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
f50a282eeee7d885
Company
Legency Rmedies Pvt. Ltd.
Type
Standard
Approval Details
Approval Id
f50a282eeee7d885
Drug Approval Philippines Name
Buderite
Product Name
Buderite
Registration Number
DRP-9170
Brand Name
Buderite
Generic Name
Budesonide
Dosage Form
Suspension for Nebulization
Dosage Strength
250mcg/mL (500mcg/2mL)
Manufacturer
Legency Rmedies Pvt. Ltd.
Importer
Suhitas Pharmaceuticals Inc.
Distributor
Preventia Healthcare Inc.
Issuance Date
25 March 2025
Expiry Date
22 September 2031
Pharmacologic Category
Glucocorticoid
Classification
Prescription Drug (Rx)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
f50a282eeee7d885
Type
Standard
Back to Philippines FDA Approvals