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Acifox - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Acifox
Approved
STANDARD
Acifox
NCPC HEBEI HUAMIN PHARMACEUTICAL CO., LTD.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
7d63971adef1d862
Company
NCPC HEBEI HUAMIN PHARMACEUTICAL CO., LTD.
Type
Standard
Approval Details
Approval Id
7d63971adef1d862
Drug Approval Philippines Name
Acifox
Product Name
Acifox
Registration Number
DR-XY47114
Brand Name
Acifox
Generic Name
Cefoxitin (As Sodium)
Dosage Form
Powder For Injection
Dosage Strength
1 g
Manufacturer
NCPC HEBEI HUAMIN PHARMACEUTICAL CO., LTD.
Importer
Aglobal Care, Inc.
Distributor
Aglobal Care, Inc.
Issuance Date
25 November 2020
Expiry Date
25 November 2025
Pharmacologic Category
Antibacterial (Cephalosporin)
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
7d63971adef1d862
Type
Standard
Back to Philippines FDA Approvals