PMDA drug package insert
カデチア配合錠LD「テバ」
PMDA Prescription drug · T'sファーマ株式会社 · package insert Sep 9, 2025
Key facts
| Brand names | カデチア配合錠LD「テバ」, カデチア配合錠HD「テバ」 |
|---|---|
| Nonproprietary names | カンデサルタン シレキセチル・ヒドロクロロチアジド配合剤 |
| Companies | 製造販売元／T'sファーマ株式会社, 販売／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 持続性アンジオテンシンⅡ受容体拮抗薬/利尿薬配合剤 |
| Therapeutic category codes | 872149 |
| YJ codes | 2149111F1044, 2149111F2040 |
| Approval numbers | 22800AMX00117, 22800AMX00118 |
| Package insert edition | 第7版 |
| Package insert date | Sep 9, 2025 |
| PMDA document key | 400813_2149111F1044_1 |
| PMDA company code | 400813 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: