PMDA drug package insert
グリセリン「東海」
PMDA Prescription drug · 東海製薬株式会社 · package insert Mar 26, 2024
Key facts
| Brand names | グリセリン「東海」 |
|---|---|
| Nonproprietary names | グリセリン |
| Companies | 製造販売元／東海製薬株式会社, 発売元／株式会社アラクス |
| Product type | Prescription drug |
| Therapeutic category | 下剤、浣腸剤 |
| Therapeutic category codes | 872357 |
| YJ codes | 2357700X1213 |
| Approval numbers | 16100AMZ01852000 |
| Package insert edition | 第1版 |
| Package insert date | Mar 26, 2024 |
| PMDA document key | 480034_2357700X1213_2 |
| PMDA company code | 480034 |
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: