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
MOVIPREP POWDER FOR ORAL SOLUTION - SFDA Drug Approval Details
Approvals
/
SFDA
/
MOVIPREP POWDER FOR ORAL SOLUTION
Authorized
NCE
MOVIPREP POWDER FOR ORAL SOLUTION
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
cd773ebcca58ad75
Company
Unknown
Type
NCE
Approval Details
Approval Id
cd773ebcca58ad75
Drug Approval Sfda Name
MOVIPREP POWDER FOR ORAL SOLUTION
Trade Name
MOVIPREP POWDER FOR ORAL SOLUTION
Generic Name
ASCORBIC ACID,SODIUM ASCORBATE,SODIUM SULFATE,MACROGOL ,POTASSIUM CHLORIDE,SODIUM CHLORIDE
Register Number
1203245038
Register Year
2017
Drug Type
NCE
Route Of Administration
Oral use
Package Type
Sachet
Package Size
2
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Uncontrolled
Storage Conditions
store below 25°c
Shelf Life
36 Months
Distribution Site
Pharmacy
Description Code
42000009380-121-100000073364
Price
44.9
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
cd773ebcca58ad75
Type
NCE
Back to SFDA Approvals