PMDA drug package insert
ユニシア配合錠LD
PMDA Prescription drug · T's製薬株式会社 · package insert Dec 24, 2025
Key facts
| Brand names | ユニシア配合錠LD, ユニシア配合錠HD |
|---|---|
| Nonproprietary names | カンデサルタン シレキセチル・アムロジピンベシル酸塩配合剤 |
| Companies | 製造販売元／T's製薬株式会社, 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/持続性Ca拮抗薬配合剤 |
| Therapeutic category codes | 872149 |
| YJ codes | 2149116F1020, 2149116F2027 |
| Approval numbers | 22200AMX00315, 22200AMX00314 |
| Package insert edition | 第5版 |
| Package insert date | Dec 24, 2025 |
| PMDA document key | 400061_2149116F1020_2 |
| PMDA company code | 400061 |
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: