PMDA drug package insert
エポエチンアルファBS注750シリンジ「JCR」
PMDA Prescription drug · JCRファーマ株式会社 · package insert Jan 21, 2026
Key facts
| Brand names | エポエチンアルファBS注750シリンジ「JCR」, エポエチンアルファBS注1500シリンジ「JCR」, エポエチンアルファBS注3000シリンジ「JCR」, エポエチンアルファBS注750「JCR」 |
|---|---|
| Nonproprietary names | エポエチン カッパ（遺伝子組換え） |
| Companies | 製造販売元／JCRファーマ株式会社, 販売元／キッセイ薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 遺伝子組換えヒトエリスロポエチン製剤 |
| Therapeutic category codes | 873999 |
| YJ codes | 3999427G1029, 3999427G2025, 3999427G3021, 3999427A1026 |
| Approval numbers | 22200AMX00238, 22200AMX00239, 22200AMX00240, 22200AMX00241 |
| Package insert edition | 第2版 |
| Package insert date | Jan 21, 2026 |
| PMDA document key | 530210_3999427A1026_1 |
| PMDA company code | 530210 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes 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: