PMDA drug package insert
デュタステリドカプセル0.5mgZA「イワキ」
PMDA Prescription drug · 岩城製薬株式会社 · package insert Feb 15, 2024
Key facts
| Brand names | デュタステリドカプセル0.5mgZA「イワキ」 |
|---|---|
| Nonproprietary names | デュタステリド |
| Companies | 製造販売元／岩城製薬株式会社 |
| 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 | 249900AM2097 |
| Approval numbers | 30300AMX00269 |
| Package insert edition | 第1版 |
| Package insert date | Feb 15, 2024 |
| PMDA document key | 130202_249900AM2097_1 |
| PMDA company code | 130202 |
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: