PMDA drug package insert

フェンタニル3日用テープ2.1mg「テイコク」

PMDA Prescription drug · 帝國製薬株式会社 · package insert Dec 24, 2024

Key facts

Brand names フェンタニル3日用テープ2.1mg「テイコク」, フェンタニル3日用テープ4.2mg「テイコク」, フェンタニル3日用テープ8.4mg「テイコク」, フェンタニル3日用テープ12.6mg「テイコク」, フェンタニル3日用テープ16.8mg「テイコク」
Nonproprietary names フェンタニル
Companies 製造販売元/帝國製薬株式会社, 販売元/テルモ株式会社
Product type Prescription drug
Therapeutic category 経皮吸収型 持続性がん疼痛治療剤
Therapeutic category codes 878219
YJ codes 8219700S5077, 8219700S6073, 8219700S7070, 8219700S8076, 8219700S9072
Approval numbers 22800AMX00453000, 22800AMX00454000, 22800AMX00455000, 22800AMX00456000, 22800AMX00457000
Package insert edition 第3版
Package insert date Dec 24, 2024
PMDA document key 470006_8219700S5077_1
PMDA company code 470006

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)