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乌美溴铵吸入粉雾剂 - NMPA Drug Approval Details
Approvals
/
NMPA
/
Umeclidinium Bromide Powder for Inhalation
Approved
化学药品
Umeclidinium Bromide Powder for Inhalation
Glaxo Group Ltd.
🇨🇳 National Medical Products Administration
Approval Date
Dec 26, 2019
Approval ID
7ucivOFN6xg
Company
Glaxo Group Ltd.
Type
化学药品
Approval Details
Approval Id
7ucivOFN6xg
Approval Number
H20190070
Generic Name
乌美溴铵吸入粉雾剂
Generic Name En
Umeclidinium Bromide Powder for Inhalation
Drug Type
化学药品
Dosage Form
吸入粉雾剂
Strength
乌美溴铵(以乌美铵计)62.5μg
Reg Date
2019-12-26
Expired Date
2024-12-25
Company Name
Glaxo Group Ltd.
Company Address
980 Great West Road, Brentford, Middlesex TW8 9GS, United Kingdom
Production Company Name
Glaxo Operations UK Ltd.
Production Company Address
Priory Street,Ware,Hertfordshire SG12 0DJ,United Kingdom
Company Detail Path
/organization/glaxo-group-ltd
Production Company Detail Path
/organization/glaxo-operations-uk-ltd
Approved
Quick Info
Agency
NMPA
Country
🇨🇳
Approval Date
Dec 26, 2019
Approval ID
7ucivOFN6xg
Type
化学药品
Back to NMPA Approvals