PMDA drug package insert
重質酸化マグネシウム「ニッコー」
PMDA Prescription drug · 日興製薬株式会社 · package insert Feb 21, 2024
Key facts
| Brand names | 重質酸化マグネシウム「ニッコー」 |
|---|---|
| Nonproprietary names | 酸化マグネシウム |
| Companies | 製造販売元／日興製薬株式会社, 発売元／中北薬品株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 制酸・緩下剤 |
| Therapeutic category codes | 872344, 872355 |
| YJ codes | 2344002X1217 |
| Approval numbers | 16000AMZ02260 |
| Package insert edition | 第1版 |
| Package insert date | Feb 21, 2024 |
| PMDA document key | 530090_2344002X1217_2 |
| PMDA company code | 530090 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: