PMDA drug package insert
リュープリンPRO注射用キット22.5mg
PMDA Prescription drug · 武田薬品工業株式会社 · package insert Sep 15, 2026
Key facts
| Brand names | リュープリンPRO注射用キット22.5mg |
|---|---|
| Nonproprietary names | リュープロレリン酢酸塩 |
| Companies | 製造販売元／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | LH-RH注1）誘導体 注1）LH-RH：黄体形成ホルモン放出ホルモン; マイクロカプセル型徐放性製剤 |
| Therapeutic category codes | 872499 |
| YJ codes | 2499407G4029 |
| Approval numbers | 22700AMX01018 |
| Package insert edition | 第2版 |
| Package insert date | Sep 15, 2026 |
| PMDA document key | 400256_2499407G4029_1 |
| PMDA company code | 400256 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: