PMDA drug package insert
ノルフロキサシン錠100mg「ツルハラ」
PMDA Prescription drug · 鶴原製薬株式会社 · package insert Jun 2, 2023
Key facts
| Brand names | ノルフロキサシン錠100mg「ツルハラ」, ノルフロキサシン錠200mg「ツルハラ」 |
|---|---|
| Nonproprietary names | ノルフロキサシン |
| Companies | 製造販売元／鶴原製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | ニューキノロン系経口抗菌剤 |
| Therapeutic category codes | 876241 |
| YJ codes | 6241005F1267, 6241005F2301 |
| Approval numbers | 22500AMX01198000, 22500AMX01199000 |
| Package insert edition | 第1版 |
| Package insert date | Jun 2, 2023 |
| PMDA document key | 460028_6241005F1267_1 |
| PMDA company code | 460028 |
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: