PMDA drug package insert

ガドテル酸メグルミン静注38%シリンジ10mL「GE」

PMDA Prescription drug · GEヘルスケアファーマ株式会社 · package insert Jan 31, 2024

Key facts

Brand names ガドテル酸メグルミン静注38%シリンジ10mL「GE」, ガドテル酸メグルミン静注38%シリンジ11mL「GE」, ガドテル酸メグルミン静注38%シリンジ13mL「GE」, ガドテル酸メグルミン静注38%シリンジ15mL「GE」, ガドテル酸メグルミン静注38%シリンジ20mL「GE」
Nonproprietary names ガドテル酸メグルミン
Companies 製造販売元/GEヘルスケアファーマ株式会社
Product type Prescription drug
Therapeutic category 環状型MRI用造影剤
Therapeutic category codes 87729
YJ codes 7290411G1049, 7290411G4030, 7290411G5036, 7290411G2045, 7290411G3041
Approval numbers 30200AMX00263000, 30200AMX00264000, 30200AMX00265000, 30200AMX00266000, 30200AMX00267000
Package insert edition 第1版
Package insert date Jan 31, 2024
PMDA document key 343048_7290411G1049_1
PMDA company code 343048

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:

Browse all PMDA approved drugs and package inserts (Japan)