PMDA drug package insert
ジーフォーＬ
PMDA OTC drug · 佐藤製薬株式会社 · package insert Mar 19, 2015
Key facts
| Brand names | ジーフォーＬ |
|---|---|
| Companies | 製造販売元／佐藤製薬株式会社 |
| Product type | OTC drug |
| OTC risk class | 第「２」類医薬品 |
| OTC dosage form | 挿入剤 |
| OTC effect category | 外用痔疾用薬 |
| Package insert date | Mar 19, 2015 |
| PMDA document key | 300089_J0801000289 |
| PMDA company code | 300089 |
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: