跳至主要内容
MedPath Trial Home
临床试验
产品
机构
资讯
AI 研究
价格
Search
EN
登录
我们重视您的隐私
我们使用 Cookie 分析网站流量并改善您的体验。请参阅我们的
隐私政策
。
拒绝
接受
ULTIBRO BREEZHALER INHALATION POWDER HARD CAPSULE 110MCG/50MCG - PPB Drug Approval Details
Approvals
/
PPB
/
ULTIBRO BREEZHALER INHALATION POWDER HARD CAPSULE 110MCG/50MCG
Approved
STANDARD
ULTIBRO BREEZHALER INHALATION POWDER HARD CAPSULE 110MCG/50MCG
NOVARTIS PHARMACEUTICALS (HK) LIMITED
🇰🇪 Pharmacy and Poisons Board
Approval Date
Jun 21, 2024
Approval ID
15e2637c925c816c
Company
NOVARTIS PHARMACEUTICALS (HK) LIMITED
Type
Standard
Approval Details
Approval Id
15e2637c925c816c
Product Name
ULTIBRO BREEZHALER INHALATION POWDER HARD CAPSULE 110MCG/50MCG
Drug Hk Name
ULTIBRO BREEZHALER INHALATION POWDER HARD CAPSULE 110MCG/50MCG
Registration Code
HK-63009
Company Name
NOVARTIS PHARMACEUTICALS (HK) LIMITED
Company Detail Path
/organization/novartis-pharmaceuticals-hk-limited
Registration Category
Part 1, Schedule 1 & Schedule 3 Poison
Sale Requirement
Prescription only Medicines
Registration Date
2014-08-26
Company Address
7/F, CITI TOWER ONE BAY EAST, 83 HOI BUN ROAD, KWUN TONG, KOWLOON
Active Ingredients
Approved
Quick Info
Agency
PPB
Country
🇰🇪
Approval Date
Jun 21, 2024
Approval ID
15e2637c925c816c
Type
Standard
Back to PPB Approvals