PMDA drug package insert
ダプトマイシン静注用350mg「サワイ」
PMDA Prescription drug · 沢井製薬株式会社 · package insert Aug 29, 2023
Key facts
| Brand names | ダプトマイシン静注用350mg「サワイ」 |
|---|---|
| Nonproprietary names | ダプトマイシン |
| Companies | 製造販売元／沢井製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 環状リポペプチド系抗生物質製剤 |
| Therapeutic category codes | 876119 |
| YJ codes | 6119402D1030 |
| Approval numbers | 30400AMX00346000 |
| Package insert edition | 第2版 |
| Package insert date | Aug 29, 2023 |
| PMDA document key | 300119_6119402D1030_1 |
| PMDA company code | 300119 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- No 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: