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
Shelogel - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Shelogel
Approved
STANDARD
Shelogel
Scheele Laboratories Phils., Inc
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
69a3cfc1642fccf9
Company
Scheele Laboratories Phils., Inc
Type
Standard
Approval Details
Approval Id
69a3cfc1642fccf9
Drug Approval Philippines Name
Shelogel
Product Name
Shelogel
Registration Number
DRP-10215
Brand Name
Shelogel
Generic Name
Aluminum Hydroxide + Magnesium
Dosage Form
Tablet
Dosage Strength
200 mg/100 mg
Manufacturer
Scheele Laboratories Phils., Inc
Issuance Date
27 February 2024
Expiry Date
02 June 2026
Pharmacologic Category
Antacid
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
69a3cfc1642fccf9
Type
Standard
Back to Philippines FDA Approvals