PMDA drug package insert
痔疾内服治療剤 痔に光
PMDA OTC drug · （名）東宝製薬 · package insert May 29, 2007
Key facts
| Brand names | 痔疾内服治療剤 痔に光 |
|---|---|
| Companies | 製造販売元／（名）東宝製薬 |
| Product type | OTC drug |
| OTC risk class | 第「２」類医薬品 |
| OTC dosage form | 錠剤 |
| OTC effect category | 内用痔疾用薬 |
| Package insert date | May 29, 2007 |
| PMDA document key | 480158_J0601003636 |
| PMDA company code | 480158 |
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: