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Strocit 2 mL - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Strocit 2 mL
Approved
STANDARD
Strocit 2 mL
Sun Pharmaceutical Medicare Limited
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
bfc2289266d1c095
Company
Sun Pharmaceutical Medicare Limited
Type
Standard
Approval Details
Approval Id
bfc2289266d1c095
Drug Approval Philippines Name
Strocit 2 mL
Product Name
Strocit 2 mL
Registration Number
DRP-8675
Brand Name
Strocit 2 mL
Generic Name
Citicoline (as Sodium)
Dosage Form
Solution For Injection (IV/IM)
Dosage Strength
250 mg /mL (500 mg/ 2 mL)
Manufacturer
Sun Pharmaceutical Medicare Limited
Importer
Sun Pharma Philippines Inc.
Distributor
Sun Pharma Philippines Inc.
Company Detail Path
/organization/sun-pharmaceutical-medicare-limited
Issuance Date
19 January 2024
Expiry Date
22 July 2029
Pharmacologic Category
Psychostimulant/Nootropic
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
bfc2289266d1c095
Type
Standard
Back to Philippines FDA Approvals