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Nexefer - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Nexefer
Approved
STANDARD
Nexefer
Theon Pharmaceuticals Limited
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
f970e5e3d8c312c4
Company
Theon Pharmaceuticals Limited
Type
Standard
Approval Details
Approval Id
f970e5e3d8c312c4
Drug Approval Philippines Name
Nexefer
Product Name
Nexefer
Registration Number
DRP-15886
Brand Name
Nexefer
Generic Name
Cefalexin (as monohydrate)
Dosage Form
Capsule
Dosage Strength
500 mg
Manufacturer
Theon Pharmaceuticals Limited
Importer
Hexagon Pharmaceuticals Limited
Distributor
Hexagon Pharmaceuticals Limited
Issuance Date
27 September 2024
Expiry Date
27 September 2029
Pharmacologic Category
Antibacterial (Cephalosporin)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
f970e5e3d8c312c4
Type
Standard
Back to Philippines FDA Approvals