PMDA drug package insert
ワンアルファ錠0.25μg
PMDA Prescription drug · 帝人ファーマ株式会社 · package insert Feb 5, 2024
Key facts
| Brand names | ワンアルファ錠0.25μg, ワンアルファ錠0.5μg, ワンアルファ錠1.0μg |
|---|---|
| Nonproprietary names | アルファカルシドール |
| Companies | 製造販売元／帝人ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 活性型ビタミンD3製剤 |
| Therapeutic category codes | 873112 |
| YJ codes | 3112001F1055, 3112001F2051, 3112001F3058 |
| Approval numbers | 22100AMX01238000, 22100AMX01237000, 22100AMX01236000 |
| Package insert edition | 第2版 |
| Package insert date | Feb 5, 2024 |
| PMDA document key | 470310_3112001F1055_1 |
| PMDA company code | 470310 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None 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: