PMDA drug package insert
ディクアノン懸濁用配合顆粒
PMDA Prescription drug · 日新製薬株式会社 · package insert Oct 28, 2024
Key facts
| Brand names | ディクアノン懸濁用配合顆粒 |
|---|---|
| Nonproprietary names | 水酸化アルミニウムゲル・水酸化マグネシウム |
| Companies | 製造販売元／日新製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 消化性潰瘍・胃炎治療剤 |
| Therapeutic category codes | 872349 |
| YJ codes | 2349101D1202 |
| Approval numbers | 22100AMX01265000 |
| Package insert edition | 第1版 |
| Package insert date | Oct 28, 2024 |
| PMDA document key | 530113_2349101D1202_1 |
| PMDA company code | 530113 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: