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Dexmedetomidine (as hydrochloride) in 0.9% Sodium Chloride - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Unknown Drug
Approved
STANDARD
Unknown Drug
Jiangsu Hengrui Medicine Co., Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
d0f77b26e1af9599
Company
Jiangsu Hengrui Medicine Co., Ltd.
Type
Standard
Approval Details
Approval Id
d0f77b26e1af9599
Drug Approval Philippines Name
Dexmedetomidine (as hydrochloride) in 0.9% Sodium Chloride
Product Name
Dexmedetomidine (as hydrochloride) in 0.9% Sodium Chloride
Registration Number
DR-XY48779
Generic Name
Dexmedetomidine (as hydrochloride) in 0.9% Sodium Chloride
Dosage Form
Solution for IV Infusion
Dosage Strength
4 mcg/mL
Manufacturer
Jiangsu Hengrui Medicine Co., Ltd.
Importer
Philcare Pharma Inc.
Distributor
Philcare Pharma Inc.
Company Detail Path
/organization/jiangsu-hengrui-medicine-co-ltd
Issuance Date
23 June 2023
Expiry Date
23 June 2028
Pharmacologic Category
Hypnotic and Sedative
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
d0f77b26e1af9599
Type
Standard
Back to Philippines FDA Approvals