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Ngenla

Active substance: somatrogon

INJECTION, SOLUTION · SOMATROGON 24 mg/1.2mL

United StatesActive

Marketing holder: Pfizer Laboratories Div Pfizer Inc

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
EU 1
  • Ngenla
    somatrogon
    EMEA/H/C/005633
    Pfizer Europe MA EEIG
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-3e12-7443-b94b-4c895d3204c2,01a1208f-559d-703c-bb4e-2f414acf96fa;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0069-0505
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 0069-0505 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0069-0505 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0069-0505 · Verified 2026-10-09 · open in source