PMDA drug package insert
フランドル錠20mg
PMDA Prescription drug · トーアエイヨー株式会社 · package insert Oct 1, 2025
Key facts
| Brand names | フランドル錠20mg |
|---|---|
| Nonproprietary names | 硝酸イソソルビド |
| Companies | 製造販売元／トーアエイヨー株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 虚血性心疾患治療剤〈持効錠〉 |
| Therapeutic category codes | 872171 |
| YJ codes | 2171011G1123 |
| Approval numbers | 21600AMZ00111000 |
| Package insert edition | 第3版 |
| Package insert date | Oct 1, 2025 |
| PMDA document key | 480008_2171011G1123_1 |
| PMDA company code | 480008 |
At a glance
- 1–9 Package insert revisions
- None 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: