PMDA drug package insert
一硝酸イソソルビド錠20mg「日新」
PMDA Prescription drug · 日新製薬株式会社 · package insert Sep 9, 2024
Key facts
| Brand names | 一硝酸イソソルビド錠20mg「日新」 |
|---|---|
| Nonproprietary names | 一硝酸イソソルビド |
| Companies | 製造販売元／日新製薬株式会社, 販売元／⽇本ジェネリック株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 狭心症治療用ISMN製剤 |
| Therapeutic category codes | 872171 |
| YJ codes | 2171023F2143 |
| Approval numbers | 23000AMX00582000 |
| Package insert edition | 第2版 |
| Package insert date | Sep 9, 2024 |
| PMDA document key | 530113_2171023F2143_1 |
| PMDA company code | 530113 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: