PMDA drug package insert
バラマイシン軟膏
PMDA Prescription drug · 東洋製薬化成株式会社 · package insert Dec 5, 2022
Key facts
| Brand names | バラマイシン軟膏 |
|---|---|
| Nonproprietary names | バシトラシン・フラジオマイシン硫酸塩 |
| Companies | 製造販売／東洋製薬化成株式会社, 販売／小野薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 化膿性皮膚疾患用剤 |
| Therapeutic category codes | 872639 |
| YJ codes | 2639805M1020 |
| Approval numbers | 13127KUZ12410001 |
| Package insert edition | 第1版 |
| Package insert date | Dec 5, 2022 |
| PMDA document key | 480199_2639805M1020_1 |
| PMDA company code | 480199 |
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: