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Latuda - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Latuda
Approved
STANDARD
Latuda
Bushu Pharmaceuticals Ltd. (Kawagoe Factory)
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
8334d07f1244e4d4
Company
Bushu Pharmaceuticals Ltd. (Kawagoe Factory)
Type
Standard
Approval Details
Approval Id
8334d07f1244e4d4
Drug Approval Philippines Name
Latuda
Product Name
Latuda
Registration Number
DR-XY48820
Brand Name
Latuda
Generic Name
Lurasidone Hydrochloride
Dosage Form
Film-Coated Tablet
Dosage Strength
20 mg
Manufacturer
Bushu Pharmaceuticals Ltd. (Kawagoe Factory)
Importer
Zuellig Pharma Corporation
Distributor
Zuellig Pharma Corporation
Issuance Date
25 July 2023
Expiry Date
25 July 2028
Classification
Prescription (Rx) Drug
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
8334d07f1244e4d4
Type
Standard
Back to Philippines FDA Approvals