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Lexofol - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Lexofol
Approved
STANDARD
Lexofol
Neon Laboratories Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
8159b53ade4e9236
Company
Neon Laboratories Ltd.
Type
Standard
Approval Details
Approval Id
8159b53ade4e9236
Drug Approval Philippines Name
Lexofol
Product Name
Lexofol
Registration Number
DRP-3206
Brand Name
Lexofol
Generic Name
Propofol
Dosage Form
Emulsion For Injection (I.V.)
Dosage Strength
10 mg/mL (1% w/v)
Manufacturer
Neon Laboratories Ltd.
Importer
Ambica International Corporation
Distributor
Delex Pharma International, Inc.
Issuance Date
29 February 2024
Expiry Date
24 August 2029
Pharmacologic Category
General Anesthetic
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
8159b53ade4e9236
Type
Standard
Back to Philippines FDA Approvals