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
NUPRO APF TOPICAL GEL - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
NUPRO APF TOPICAL GEL
Authorized
STANDARD
NUPRO APF TOPICAL GEL
DENTSPLY INTERNATIONAL
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
3b6ced43381679f2
Company
DENTSPLY INTERNATIONAL
Type
Standard
Approval Details
Approval Id
3b6ced43381679f2
Drug Approval Canada Name
NUPRO APF TOPICAL GEL
Product Name
NUPRO APF TOPICAL GEL
Status
Cancelled Post Market
Status Date
2008-06-20
Original Market Date
1995-12-31
Din
02050269
Drug Class
Human
Dosage Form
Gel
Route Of Administration
Topical
Schedule
OTC
Ahfs
34:00.00
Atc Original
A01AA51 SODIUM FLUORIDE, COMBINATIONS
Atc Name
a 01 aa 51
Aig Number
0207164005
Company Name
DENTSPLY INTERNATIONAL
Company Address
60, 221 West Philadelphia Street, York, Pennsylvania, United States, 17401
Company Detail Path
/organization/dentsply-international
Company Information
Pharmaceutical Company Name
DENTSPLY INTERNATIONAL
Country Name
United States
Province Name
Florida
City Name
tampa,florida,country_us
Address
6015 Benjamin Rd
Active Ingredients
SODIUM FLUORIDE
2.59 %
PHOSPHORIC ACID
1.16 %
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
3b6ced43381679f2
Type
Standard
Back to Health Canada Approvals