PMDA drug package insert
エラプレース点滴静注液6mg
PMDA Prescription drug · サノフィ株式会社 · package insert Dec 12, 2023
Key facts
| Brand names | エラプレース点滴静注液6mg |
|---|---|
| Nonproprietary names | イデュルスルファーゼ（遺伝子組換え） |
| Companies | 製造販売業者／サノフィ株式会社, 製造元／Shire Human Genetic Therapies, Inc., 米国 |
| Product type | Prescription drug |
| Therapeutic category | 遺伝子組換えムコ多糖症II型治療剤 |
| Therapeutic category codes | 873959 |
| YJ codes | 3959413A1029 |
| Approval numbers | 21900AMX01739 |
| Package insert edition | 第2版 |
| Package insert date | Dec 12, 2023 |
| PMDA document key | 780069_3959413A1029_2 |
| PMDA company code | 780069 |
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: