PMDA drug package insert
メホビル配合錠LD「日新」
PMDA Prescription drug · 日新製薬株式会社 · package insert Oct 30, 2025
Key facts
| Brand names | メホビル配合錠LD「日新」, メホビル配合錠HD「日新」 |
|---|---|
| Nonproprietary names | ビルダグリプチン・メトホルミン塩酸塩配合剤 |
| Companies | 製造販売元／日新製薬株式会社, 販売元／高田製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 選択的DPP-4阻害薬/ビグアナイド系薬配合剤 ［2型糖尿病治療薬］ |
| Therapeutic category codes | 873969 |
| YJ codes | 3969104F1045, 3969104F2041 |
| Approval numbers | 30700AMX00041, 30700AMX00042 |
| Package insert edition | 第2版 |
| Package insert date | Oct 30, 2025 |
| PMDA document key | 530113_3969104F1045_2 |
| PMDA company code | 530113 |
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: