PMDA drug package insert
ブレオ注射用5mg
PMDA Prescription drug · 日本化薬株式会社 · package insert Oct 26, 2023
Key facts
| Brand names | ブレオ注射用5mg, ブレオ注射用15mg |
|---|---|
| Nonproprietary names | ブレオマイシン塩酸塩 |
| Companies | 製造販売元／日本化薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 抗腫瘍性抗生物質 |
| Therapeutic category codes | 874234 |
| YJ codes | 4234400D4032, 4234400D5039 |
| Approval numbers | 21800AMX10209, 21800AMX10210 |
| Package insert edition | 第1版 |
| Package insert date | Oct 26, 2023 |
| PMDA document key | 530191_4234400D4032_1 |
| PMDA company code | 530191 |
At a glance
- 1–9 Package insert revisions
- 1–9 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: