PMDA drug package insert
新セイムビタンゴールド
PMDA OTC drug · 東和製薬株式会社 · package insert Oct 15, 2025
Key facts
| Brand names | 新セイムビタンゴールド |
|---|---|
| Companies | 製造販売元／東和製薬株式会社 |
| Product type | OTC drug |
| OTC risk class | 第３類医薬品 |
| OTC dosage form | カプセル |
| OTC effect category | ビタミンB1主薬製剤 |
| Package insert date | Oct 15, 2025 |
| PMDA document key | 480232_J1001000073 |
| PMDA company code | 480232 |
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: