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Apidra

Wirkstoff: insulin glulisine

insulin glulisine

Zentrale EU-ZulassungAktiv

Zulassungsinhaber: sanofi-aventis Deutschland GmbH

Geprüft 2026-10-09 · EMA

Äquivalente in anderen Ländern
Zusammensetzung
Äquivalente nach Ländern

Arzneimittel mit demselben Wirkstoff, die in anderen Ländern zugelassen sind.

LandArzneimittel
US 6
  • Apidra
    Injektionslösung [Übersetzung der Form; Original: INJECTION, SOLUTION (openFDA)] · INSULIN GLULISINE 100 [iU]/mL
    0088-2500
    sanofi-aventis U.S. LLC
  • Apidra SoloStar
    Injektionslösung [Übersetzung der Form; Original: INJECTION, SOLUTION (openFDA)] · INSULIN GLULISINE 100 [iU]/mL
    0088-2502
    sanofi-aventis U.S. LLC
  • Attention Deficit Mild Drops 2146
    Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · .GAMMA.-AMINOBUTYRIC ACID 3 [hp_X]/59mL, GINKGO 3 [hp_X]/59mL, BOS TAURUS BRAIN 6 [hp_X]/59mL, BOS TAURUS HYPOTHALAMUS 6 [hp_X]/59mL, BEEF KIDNEY 6 [hp_X]/59mL, BEEF LIVER 6 [hp_X]/59mL, BOS TAURUS PANCREAS 6 [hp_X]/59mL, SUS SCROFA PINEAL GLAND 6 [hp_X]/59mL, SILVER NITRATE 30 [hp_X]/59mL, AMARYLLIS BELLADONNA WHOLE 30 [hp_X]/59mL, COFFEA ARABICA SEED, ROASTED 30 [hp_X]/59mL, PHOSPHORUS 30 [hp_X]/59mL, AMBERGRIS 30 [hp_X]/59mL, BARIUM CARBONATE 30 [hp_X]/59mL, BARIUM CHLORIDE DIHYDRATE 30 [hp_X]/59mL, INSULIN GLULISINE 30 [hp_X]/59mL, LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/59mL, GONORRHEAL URETHRAL SECRETION HUMAN 30 [hp_X]/59mL, DATURA STRAMONIUM 30 [hp_X]/59mL, THUJA OCCIDENTALIS LEAF 30 [hp_X]/59mL, BOVINE TUBERCULIN 30 [hp_X]/59mL, VERATRUM ALBUM ROOT 30 [hp_X]/59mL
    63083-2146
    Professional Complementary Health Formulas
  • Attention Deficit Severe Drops 2147
    Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · .GAMMA.-AMINOBUTYRIC ACID 3 [hp_X]/59mL, GINKGO 3 [hp_X]/59mL, BOS TAURUS BRAIN 6 [hp_X]/59mL, BOS TAURUS HYPOTHALAMUS 6 [hp_X]/59mL, BEEF KIDNEY 6 [hp_X]/59mL, BEEF LIVER 6 [hp_X]/59mL, BOS TAURUS PANCREAS 6 [hp_X]/59mL, SUS SCROFA PINEAL GLAND 6 [hp_X]/59mL, SILVER NITRATE 30 [hp_X]/59mL, COFFEA ARABICA SEED, ROASTED 30 [hp_X]/59mL, LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/59mL, AMARYLLIS BELLADONNA WHOLE 60 [hp_X]/59mL, PHOSPHORUS 60 [hp_X]/59mL, AMBERGRIS 60 [hp_X]/59mL, BARIUM CARBONATE 60 [hp_X]/59mL, BARIUM CHLORIDE DIHYDRATE 60 [hp_X]/59mL, BUFO BUFO CUTANEOUS GLAND 60 [hp_X]/59mL, HYOSCYAMUS NIGER 60 [hp_X]/59mL, GONORRHEAL URETHRAL SECRETION HUMAN 60 [hp_X]/59mL, DATURA STRAMONIUM 60 [hp_X]/59mL, LYCOSA TARANTULA 60 [hp_X]/59mL, THUJA OCCIDENTALIS LEAF 60 [hp_X]/59mL, BOVINE TUBERCULIN 60 [hp_X]/59mL, VERATRUM ALBUM ROOT 60 [hp_X]/59mL, INSULIN GLULISINE 60 [hp_X]/59mL
    63083-2147
    Professional Complementary Health Formulas
  • DNA Insulin Drops 2019
    Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · CHROMIUM 6 [hp_X]/59mL, LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/59mL, VANADIUM 6 [hp_X]/59mL, PANCRELIPASE AMYLASE 6 [hp_X]/59mL, INSULIN GLULISINE 12 [hp_X]/59mL, PHOSPHORIC ACID 30 [hp_X]/59mL, URANYL NITRATE HEXAHYDRATE 30 [hp_X]/59mL, RADIUM BROMIDE 60 [hp_X]/59mL
    63083-2019
    Professional Complementary Health Formulas
Alle Arzneimittel in diesem Land (6)
Einfuhr und Kontrolle

Kontrolle nach Ländern

  • Vereinigte Staatennur auf Rezept

    Quelle: openFDA NDC · Datensatz 01a12093-43de-75ba-96c0-94a07d773e91,01a12095-758b-74fa-837e-fea58c09cf9c;count=2 · gültig ab 2026-10-09 · geprüft 2026-10-09

Mehr zum Kontrollstatus
Zulassung
Zulassungsnummer
EMEA/H/C/000557
Zulassungsstatus
Aktiv
ATC-Code
A10AB06
Quellen
  • product · EMA · EMEA/H/C/000557 · Geprüft 2026-10-09
  • registration_status · EMA · EMEA/H/C/000557 · Geprüft 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/000557 · Geprüft 2026-10-09