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Ceftris - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Ceftris
Approved
STANDARD
Ceftris
Venus Remedies. Limited
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
9be1e120c4b6f18d
Company
Venus Remedies. Limited
Type
Standard
Approval Details
Approval Id
9be1e120c4b6f18d
Drug Approval Philippines Name
Ceftris
Product Name
Ceftris
Registration Number
DRP-16470
Brand Name
Ceftris
Generic Name
Ceftriaxone (as sodium) + Sulbactam (as sodium)
Dosage Form
Powder for Injection (IM/IV)
Dosage Strength
1 g/500 mg
Manufacturer
Venus Remedies. Limited
Importer
Despina Pharma Inc.
Distributor
Despina Pharma Inc.
Issuance Date
25 March 2025
Expiry Date
25 March 2030
Pharmacologic Category
Antibacterial (Third-generation cephalosporin)
Classification
Prescription (Rx) Drug
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
9be1e120c4b6f18d
Type
Standard
Back to Philippines FDA Approvals