PMDA drug package insert
ベタメタゾン吉草酸エステルローション0.12%「イワキ」
PMDA Prescription drug · 岩城製薬株式会社 · package insert Feb 22, 2023
Key facts
| Brand names | ベタメタゾン吉草酸エステルローション0.12%「イワキ」 |
|---|---|
| Nonproprietary names | ベタメタゾン吉草酸エステル |
| Companies | 製造販売元／岩城製薬株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 副腎皮質ホルモン外用剤 |
| Therapeutic category codes | 872646 |
| YJ codes | 2646701Q1054 |
| Approval numbers | 30100AMX00354 |
| Package insert edition | 第1版 |
| Package insert date | Feb 22, 2023 |
| PMDA document key | 130202_2646701Q1054_1 |
| PMDA company code | 130202 |
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: