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Active substance: ceftaroline fosamil

ceftaroline fosamil

Centralised EU authorisationActive

Marketing holder: Pfizer Ireland Pharmaceuticals

Verified 2026-10-09 · EMA

Analogues in other countries
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 6
  • Ceftaroline Fosamil
    INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · CEFTAROLINE FOSAMIL 600 mg/20mL
    60505-6125
    Apotex Corp.
  • Ceftaroline Fosamil
    INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · CEFTAROLINE FOSAMIL 600 mg/20mL
    60505-4947
    Apotex Corp.
  • Ceftaroline Fosamil
    INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · CEFTAROLINE FOSAMIL 400 mg/20mL
    60505-6124
    Apotex Corp.
  • Ceftaroline Fosamil
    INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · CEFTAROLINE FOSAMIL 400 mg/20mL
    60505-4946
    Apotex Corp.
  • Teflaro
    POWDER, FOR SOLUTION · CEFTAROLINE FOSAMIL 400 mg/20mL
    0456-0400
    Allergan, Inc.
All products in this country (6)
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12092-025a-7a32-a498-bbf167dfa617,01a12093-e9d1-716a-9aba-6338f18cbeea,01a12093-e9e9-7691-b5fc-540a5114f545,01a12095-0d55-75e4-ab06-884ad5bdb72c,01a12095-0e29-72df-b3ad-7e4db2682df7;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/002252
Registration status
Active
ATC code
J01DI02
Sources
  • product · EMA · EMEA/H/C/002252 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/002252 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/002252 · Verified 2026-10-09