PMDA drug package insert
グリメピリド錠0.5mg「AA」
PMDA Prescription drug · あすか製薬株式会社 · package insert Jan 31, 2025
Key facts
| Brand names | グリメピリド錠0.5mg「AA」, グリメピリド錠1mg「AA」, グリメピリド錠3mg「AA」 |
|---|---|
| Nonproprietary names | グリメピリド |
| Companies | 製造販売元／あすか製薬株式会社, 販売元／武田薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | スルホニルウレア系経口血糖降下剤 |
| Therapeutic category codes | 873961 |
| YJ codes | 3961008F3082, 3961008F1039, 3961008F2035 |
| Approval numbers | 22400AMX00411, 22200AMX00544, 22200AMX00545 |
| Package insert edition | 第2版 |
| Package insert date | Jan 31, 2025 |
| PMDA document key | 470007_3961008F1039_1 |
| PMDA company code | 470007 |
At a glance
- 1–9 Package insert revisions
- 10–99 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: