PMDA drug package insert
クエン酸水和物原末「ニッコー」
PMDA Prescription drug · 日興製薬株式会社 · package insert Jan 10, 2024
Key facts
| Brand names | クエン酸水和物原末「ニッコー」 |
|---|---|
| Nonproprietary names | クエン酸水和物 |
| Companies | 製造販売元／日興製薬株式会社, 発売元／日興製薬販売株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 緩衝・矯味剤 |
| Therapeutic category codes | 877149 |
| YJ codes | 7149007X1234 |
| Approval numbers | 22200AMX00386 |
| Package insert edition | 第1版 |
| Package insert date | Jan 10, 2024 |
| PMDA document key | 530090_7149007X1234_2 |
| PMDA company code | 530090 |
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: