PMDA drug package insert
デキサンVG軟膏0.12%
PMDA Prescription drug · 富士製薬工業株式会社 · package insert Jan 31, 2024
Key facts
| Brand names | デキサンVG軟膏0.12% |
|---|---|
| Nonproprietary names | ベタメタゾン吉草酸エステル・ゲンタマイシン硫酸塩 |
| Companies | 製造販売元／富士製薬工業株式会社, 販売元／日医工株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 皮膚外用合成副腎皮質ホルモン・抗生物質配合剤 |
| Therapeutic category codes | 872647 |
| YJ codes | 2647709M1137 |
| Approval numbers | 22000AMX00919 |
| Package insert edition | 第1版 |
| Package insert date | Jan 31, 2024 |
| PMDA document key | 670109_2647709M1137_2 |
| PMDA company code | 670109 |
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: