Alfuzosin Hydrochloride
Active substance: alfuzosin
TABLET, FILM COATED, EXTENDED RELEASE · ALFUZOSIN HYDROCHLORIDE 10 mg/1
United StatesActive
Marketing holder: Rising Pharma Holdings, Inc.
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
- ALFUZOSIN HYDROCHLORIDE · 10 mg/1
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 7 |
|
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-49b4-71fa-bc37-2b1bb6af7a4a,01a120c4-b2d0-79b6-bda6-011a4f67a57b,01a120c4-d39e-715b-a72c-b75777262ea5,01a120c4-d695-70b9-a9c3-85991f561266,01a120c5-a3d5-76c3-8d54-ed8fbaafca41;count=5 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-2947-72f1-ba49-cb78d7857707,01a1208d-560e-7818-81c5-acb97b0a895c,01a1208d-6ff5-70e7-a9c6-96b251fb85d1,01a1208d-b1f8-7817-a880-1d265a63968f,01a1208e-69a8-7db6-aa7c-18781e39b935;count=17 · valid from 2026-10-09 · verified 2026-10-09
- Registration number
- 57237-114
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
- product · openFDA NDC · 57237-114 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 57237-114 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 57237-114 · Verified 2026-10-09 · open in source