FENOFIBRATE
Active substance: fenofibrate
TABLET · FENOFIBRATE 54 mg/1
United StatesActive
Marketing holder: NorthStar RxLLC
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
- FENOFIBRATE · 54 mg/1
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 13 |
|
| EU 3 |
|
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-4f13-741b-958c-c5bff3e06993,01a120c3-a626-7f6b-801c-a38f8f653700,01a120c3-aca9-7b6b-a3c0-3b4650813038,01a120c3-b41e-73eb-87fe-3ac1fc1f8084,01a120c4-c6d1-7750-be05-aae2d7c55b26;count=9 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-2cd3-7710-97f5-eff2550a2268,01a1208c-2d13-78f7-962d-a913a881b903,01a1208c-3665-741a-b4b8-396a33b20136,01a1208c-51fb-753a-a61f-f29eccd41911,01a1208c-5dd8-71e8-9a7f-5aa85af70879;count=212 · valid from 2026-10-09 · verified 2026-10-09
- Registration number
- 72603-840
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
- product · openFDA NDC · 72603-840 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 72603-840 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 72603-840 · Verified 2026-10-09 · open in source