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Philippines FDA
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Zolopat Forte
Approved
STANDARD
Zolopat Forte
Remington Pharmaceuticals Industries (Pvt/) Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
38af095525a1c269
Company
Remington Pharmaceuticals Industries (Pvt/) Ltd.
Type
Standard
Approval Details
Approval Id
38af095525a1c269
Drug Approval Philippines Name
Zolopat Forte
Product Name
Zolopat Forte
Registration Number
DRP-12249
Brand Name
Zolopat Forte
Generic Name
Olopatadine (as hydrochloride)
Dosage Form
Ophthalmic Solution (Eye Drops)
Dosage Strength
2mg/mL
Manufacturer
Remington Pharmaceuticals Industries (Pvt/) Ltd.
Importer
Opthamed Pharma Corp
Distributor
Opthamed Pharma Corp.
Issuance Date
25 August 2024
Expiry Date
13 March 2030
Pharmacologic Category
Antihistamine
Classification
Prescription Drug (Rx)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
38af095525a1c269
Type
Standard
Back to Philippines FDA Approvals
Zolopat Forte - Philippines FDA Drug Approval Details