PMDA drug package insert
Ｖロートナイトプレミアム アイ内服薬
PMDA OTC drug · ロート製薬株式会社 · package insert Jan 19, 2023
Key facts
| Brand names | Ｖロートナイトプレミアム アイ内服薬 |
|---|---|
| Companies | 製造販売元／ロート製薬株式会社 |
| Product type | OTC drug |
| OTC risk class | 第「２」類医薬品 |
| OTC dosage form | カプセル |
| OTC effect category | ビタミンAD主薬製剤 |
| Package insert date | Jan 19, 2023 |
| PMDA document key | 880020_K2301000002 |
| PMDA company code | 880020 |
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: