PMDA drug package insert
酸化マグネシウム細粒83%〈ハチ〉
PMDA Prescription drug · 東洋製薬化成株式会社 · package insert Sep 13, 2023
Key facts
| Brand names | 酸化マグネシウム細粒83%〈ハチ〉 |
|---|---|
| Nonproprietary names | 酸化マグネシウム |
| Companies | 製造販売元／東洋製薬化成株式会社, 発売元／丸石製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 制酸剤，緩下剤 |
| Therapeutic category codes | 872344, 872355 |
| YJ codes | 2344009C1047 |
| Approval numbers | 22500AMX00115 |
| Package insert edition | 第1版 |
| Package insert date | Sep 13, 2023 |
| PMDA document key | 480199_2344009C1047_1 |
| PMDA company code | 480199 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 Safety communications
- No PMDA review report published
- No Risk management plan (RMP)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA approved drugs and package inserts (Japan)
Japan's PMDA publishes the package insert (添付文書) of every prescription drug, OTC drug and regenerative medical product, with brand and nonproprietary names, YJ codes and approval numbers. Names appear in Japanese as published.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, package insert database · Source date: