PMDA drug package insert
メイアクトMS錠100mg
PMDA Prescription drug · Meiji Seika ファルマ株式会社 · package insert Dec 17, 2021
Key facts
| Brand names | メイアクトMS錠100mg |
|---|---|
| Nonproprietary names | セフジトレン ピボキシル |
| Companies | 製造販売元／Meiji Seika ファルマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 経口用セフェム系抗生物質製剤 |
| Therapeutic category codes | 876132 |
| YJ codes | 6132015F1037 |
| Approval numbers | 21700AMZ00757000 |
| Package insert edition | 第1版 |
| Package insert date | Dec 17, 2021 |
| PMDA document key | 780009_6132015F1037_1 |
| PMDA company code | 780009 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- 1–9 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: