PMDA drug package insert
ジェイゾロフト錠25mg
PMDA Prescription drug · ヴィアトリス製薬合同会社 · package insert Jul 1, 2024
Key facts
| Brand names | ジェイゾロフト錠25mg, ジェイゾロフト錠50mg, ジェイゾロフト錠100mg, ジェイゾロフトOD錠25mg, ジェイゾロフトOD錠50mg, ジェイゾロフトOD錠100mg |
|---|---|
| Nonproprietary names | セルトラリン塩酸塩 |
| Companies | 製造販売元／ヴィアトリス製薬合同会社 |
| Product type | Prescription drug |
| Therapeutic category | 選択的セロトニン再取り込み阻害剤 |
| Therapeutic category codes | 871179 |
| YJ codes | 1179046F1028, 1179046F2024, 1179046F3020, 1179046F4027, 1179046F5023, 1179046F6020 |
| Approval numbers | 21800AMZ10353, 21800AMZ10354, 22600AMX00514, 22600AMX00868, 22600AMX00869, 22600AMX00870 |
| Package insert edition | 第6版 |
| Package insert date | Jul 1, 2024 |
| PMDA document key | 671450_1179046F1028_4 |
| PMDA company code | 671450 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: