PMDA drug package insert
ベナゼプリル塩酸塩錠2.5mg「サワイ」
PMDA Prescription drug · 沢井製薬株式会社 · package insert Jan 24, 2024
Key facts
| Brand names | ベナゼプリル塩酸塩錠2.5mg「サワイ」, ベナゼプリル塩酸塩錠5mg「サワイ」, ベナゼプリル塩酸塩錠10mg「サワイ」 |
|---|---|
| Nonproprietary names | ベナゼプリル塩酸塩 |
| Companies | 製造販売元／沢井製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | アンジオテンシン変換酵素阻害剤 |
| Therapeutic category codes | 872144 |
| YJ codes | 2144007F1051, 2144007F2066, 2144007F3054 |
| Approval numbers | 22600AMX00838000, 22600AMX00839000, 22600AMX00840000 |
| Package insert edition | 第1版 |
| Package insert date | Jan 24, 2024 |
| PMDA document key | 300119_2144007F1051_1 |
| PMDA company code | 300119 |
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: