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Aurosol - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Aurosol
Approved
STANDARD
Aurosol
Aurolab
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
3f59747e24eb23c1
Company
Aurolab
Type
Standard
Approval Details
Approval Id
3f59747e24eb23c1
Drug Approval Philippines Name
Aurosol
Product Name
Aurosol
Registration Number
DRP-5157
Brand Name
Aurosol
Generic Name
Hypromellose
Dosage Form
Ophthalmic Solution
Dosage Strength
7mg/mL (0.7%W/V)
Manufacturer
Aurolab
Importer
Brady Pharma Inc.
Distributor
Brady Pharma Inc.
Company Detail Path
/organization/aurolab-trust
Issuance Date
20 January 2023
Expiry Date
06 March 2028
Pharmacologic Category
Ophthalmic Lubricant
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
3f59747e24eb23c1
Type
Standard
Back to Philippines FDA Approvals