PMDA drug package insert
エネーボ配合経腸用液
PMDA Prescription drug · アボットジャパン合同会社 · package insert Dec 21, 2023
Key facts
| Brand names | エネーボ配合経腸用液 |
|---|---|
| Nonproprietary names | 経腸成分栄養剤 |
| Companies | 製造販売元／アボットジャパン合同会社 |
| Product type | Prescription drug |
| Therapeutic category | たん白アミノ酸製剤 |
| Therapeutic category codes | 873259 |
| YJ codes | 3259119S1029 |
| Approval numbers | 22600AMX00527000 |
| Package insert edition | 第1版 |
| Package insert date | Dec 21, 2023 |
| PMDA document key | 100159_3259119S1029_1 |
| PMDA company code | 100159 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: