PMDA drug package insert

メマンチン塩酸塩錠5mg「アメル」

PMDA Prescription drug · 共和薬品工業株式会社 · package insert Jul 17, 2024

Key facts

Brand names メマンチン塩酸塩錠5mg「アメル」, メマンチン塩酸塩錠10mg「アメル」, メマンチン塩酸塩錠20mg「アメル」, メマンチン塩酸塩OD錠5mg「アメル」, メマンチン塩酸塩OD錠10mg「アメル」, メマンチン塩酸塩OD錠20mg「アメル」
Nonproprietary names メマンチン塩酸塩
Companies 製造販売元/共和薬品工業株式会社
Product type Prescription drug
Therapeutic category NMDA受容体拮抗 アルツハイマー型認知症治療剤
Therapeutic category codes 87119
YJ codes 1190018F1066, 1190018F2062, 1190018F3069, 1190018F4103, 1190018F5100, 1190018F6106
Approval numbers 30200AMX00260, 30200AMX00261, 30200AMX00262, 30200AMX00180, 30200AMX00181, 30200AMX00182
Package insert edition 第1版
Package insert date Jul 17, 2024
PMDA document key 672173_1190018F1066_2
PMDA company code 672173

At a glance

  • 1–9 Package insert revisions
  • 10–99 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:

Browse all PMDA approved drugs and package inserts (Japan)