PMDA drug package insert
アンナザルベ・エース
PMDA OTC drug · エスエス製薬(株) · package insert May 31, 2018
Key facts
| Brand names | アンナザルベ・エース |
|---|---|
| Companies | 製造販売元／エスエス製薬(株) |
| Product type | OTC drug |
| OTC risk class | 第２類医薬品 |
| OTC dosage form | 塗布剤 |
| OTC effect category | 化膿性疾患用薬 |
| Package insert date | May 31, 2018 |
| PMDA document key | 170039_J0601006247 |
| PMDA company code | 170039 |
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: