PMDA drug package insert
デュタステリドカプセル0.5mgZA「ANG」
PMDA Prescription drug · アンファー製薬株式会社 · package insert Jan 30, 2025
Key facts
| Brand names | デュタステリドカプセル0.5mgZA「ANG」 |
|---|---|
| Nonproprietary names | デュタステリド |
| Companies | 製造販売元／アンファー製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 5α還元酵素1型/2型阻害薬; 男性型脱毛症治療薬 |
| Therapeutic category codes | 87249 |
| YJ codes | 249900AM2119 |
| Approval numbers | 30600AMX00170000 |
| Package insert edition | 第2版 |
| Package insert date | Jan 30, 2025 |
| PMDA document key | 113167_249900AM2119_1 |
| PMDA company code | 113167 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: