Renflexis
Active substance: infliximab
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INFLIXIMAB 100 mg/1
United StatesActive
Marketing holder: Organon LLC
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
- INFLIXIMAB · 100 mg/1
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 6 |
|
| EU 7 |
|
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-4ab0-793f-8be1-17ebb27e0618,01a120c3-7eca-7c0e-b085-c14f4422e422,01a120c4-d303-76d8-a199-66fc311e5913,01a120c5-1473-75c2-96c2-a1834ea4c0f9,01a120c5-c373-72df-9357-629eb29a3d47;count=5 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-7bec-7927-901a-a83670c22876,01a1208f-1bf2-709b-bfc8-23d7980fa869,01a1208f-5c9a-7822-9f71-41a72176c0ea,01a12098-d6cf-72a8-a867-60e290c41824,01a1209b-3cac-7e6f-a9ae-4f1bf648cdf6;count=5 · valid from 2026-10-09 · verified 2026-10-09
- Registration number
- 78206-162
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAVENOUS
- product · openFDA NDC · 78206-162 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 78206-162 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 78206-162 · Verified 2026-10-09 · open in source