PMDA drug package insert

アダリムマブBS皮下注20mgシリンジ0.2mL「CTNK」

PMDA Prescription drug · 日本化薬株式会社 · package insert Mar 25, 2026

Key facts

Brand names アダリムマブBS皮下注20mgシリンジ0.2mL「CTNK」, アダリムマブBS皮下注40mgシリンジ0.4mL「CTNK」, アダリムマブBS皮下注80mgシリンジ0.8mL「CTNK」, アダリムマブBS皮下注40mgペン0.4mL「CTNK」, アダリムマブBS皮下注80mgペン0.8mL「CTNK」
Nonproprietary names アダリムマブ(遺伝子組換え)
Companies 製造販売元(輸入)/日本化薬株式会社, 提携先/セルトリオン・ヘルスケア・ジャパン株式会社
Product type Prescription drug
Therapeutic category ヒト型抗ヒトTNFαモノクローナル抗体製剤
Therapeutic category codes 873999
YJ codes 3999472G1024, 3999472G2020, 3999472G3027, 3999472G4023, 3999472G5020
Approval numbers 30500AMX00239, 30500AMX00240, 30500AMX00241, 30500AMX00242, 30500AMX00243
Package insert edition 第6版
Package insert date Mar 25, 2026
PMDA document key 530191_3999472G1024_1
PMDA company code 530191

At a glance

  • 1–9 Package insert revisions
  • 10–99 Related PMDA documents
  • None Safety communications
  • Yes PMDA review report published
  • Yes 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:

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