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Luprolex - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Luprolex
Approved
STANDARD
Luprolex
Takeda Pharmaceutical Co. Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
474b46b674345391
Company
Takeda Pharmaceutical Co. Ltd.
Type
Standard
Approval Details
Approval Id
474b46b674345391
Drug Approval Philippines Name
Luprolex
Product Name
Luprolex
Registration Number
DR-XY20801
Brand Name
Luprolex
Generic Name
Leuprorelin Acetate
Dosage Form
Powder For Injection (Im/Sc) Sustained Release
Dosage Strength
1.88mg
Manufacturer
Takeda Pharmaceutical Co. Ltd.
Importer
Takeda Healthcare Philippines, Inc.
Issuance Date
29 December 2020
Expiry Date
19 January 2026
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
474b46b674345391
Type
Standard
Back to Philippines FDA Approvals