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Betahiz - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Betahiz
Approved
STANDARD
Betahiz
Unison Pharmaceuticals Private Limited.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
073dd2973227cdbf
Company
Unison Pharmaceuticals Private Limited.
Type
Standard
Approval Details
Approval Id
073dd2973227cdbf
Drug Approval Philippines Name
Betahiz
Product Name
Betahiz
Registration Number
DRP-16049
Brand Name
Betahiz
Generic Name
Betahistine dihydrochloride
Dosage Form
Tablet
Dosage Strength
16 mg
Manufacturer
Unison Pharmaceuticals Private Limited.
Importer
Euroasia Pharmaceuticals, Inc
Distributor
Euroasia Pharmaceuticals, Inc
Issuance Date
28 October 2024
Expiry Date
28 October 2029
Pharmacologic Category
Anti-vertigo
Classification
Prescription (Rx) Drug
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
073dd2973227cdbf
Type
Standard
Back to Philippines FDA Approvals