PMDA drug package insert
セピエンス顆粒分包250mg
PMDA Prescription drug · PTCセラピューティクス株式会社 · package insert Mar 18, 2026
Key facts
| Brand names | セピエンス顆粒分包250mg, セピエンス顆粒分包1000mg |
|---|---|
| Nonproprietary names | セピアプテリン |
| Companies | 製造販売元／PTCセラピューティクス株式会社 |
| Product type | Prescription drug |
| Therapeutic category | フェニルケトン尿症治療剤 |
| Therapeutic category codes | 873999 |
| YJ codes | 3999067D1024, 3999067D2020 |
| Approval numbers | 30700AMX00267000, 30700AMX00268000 |
| Package insert edition | 第2版 |
| Package insert date | Mar 18, 2026 |
| PMDA document key | 651427_3999067D1024_1 |
| PMDA company code | 651427 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: