DEA schedule
Is alfuzosin a controlled substance?
Federal schedule for alfuzosin from the FDA NDC directory, checked against the DEA controlled substances list.
Source: FDA NDC Directory file dated 2026-10-22. Publisher page
No. Alfuzosin is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and alfuzosin is not on the DEA controlled substances list.
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Schedule check
| Source | What it lists |
|---|---|
| FDA NDC directory | 17 prescription listings from 11 labelers, none with a DEA schedule |
| DEA controlled substances list | alfuzosin is not on the list |
Alfuzosin NDC listings
| NDC | Product | Form | Strength | Labeler | DEA schedule |
|---|---|---|---|---|---|
| 59212-200 | Uroxatral | tablet, extended release | 10 mg/1 | Advanz Pharma (US) Corp. | None |
| 69097-844 | Alfuzosin Hydrochloride extended release | tablet | 10 mg/1 | Cipla USA Inc. | None |
| 29300-155 | Alfuzosin hydrochloride | tablet, extended release | 10 mg/1 | Unichem Pharmaceuticals (USA), Inc. | None |
| 43353-945 | Alfuzosin hydrochloride | tablet, extended release | 10 mg/1 | Aphena Pharma Solutions - Tennessee, LLC | None |
| 47335-956 | Alfuzosin Hydrochloride | tablet, extended release | 10 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 51655-432 | Alfuzosin Hydrochloride | tablet, extended release | 10 mg/1 | Northwind Health Company, LLC | None |
| 51655-967 | Alfuzosin hydrochloride | tablet, extended release | 10 mg/1 | Northwind Health Company, LLC | None |
| 60505-2850 | Alfuzosin Hydrochloride | tablet, extended release | 10 mg/1 | Apotex Corp. | None |
| 63629-9155 | Alfuzosin hydrochloride | tablet, extended release | 10 mg/1 | Bryant Ranch Prepack | None |
| 71335-2146 | Alfuzosin Hydrochloride | tablet, extended release | 10 mg/1 | Bryant Ranch Prepack | None |
| 72162-1449 | Alfuzosin Hydrochloride | tablet, extended release | 10 mg/1 | Bryant Ranch Prepack | None |
| 76282-302 | Alfuzosin hydrochloride | tablet, extended release | 10 mg/1 | Exelan Pharmaceuticals Inc. | None |
| 51655-087 | Alfuzosin Hydrochloride | tablet, film coated, extended release | 10 mg/1 | Northwind Health Company, LLC | None |
| 57237-114 | Alfuzosin Hydrochloride | tablet, film coated, extended release | 10 mg/1 | Rising Pharma Holdings, Inc. | None |
| 65862-249 | Alfuzosin Hydrochloride | tablet, film coated, extended release | 10 mg/1 | Aurobindo Pharma Limited | None |
| 71335-2578 | Alfuzosin Hydrochloride | tablet, film coated, extended release | 10 mg/1 | Bryant Ranch Prepack | None |
| 84386-153 | Alfuzosin Hydrochloride | tablet, film coated, extended release | 10 mg/1 | Aurobindo Pharma Limited | None |
Questions
Is alfuzosin a controlled substance?
No. Alfuzosin is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and alfuzosin is not on the DEA controlled substances list.
Is alfuzosin a narcotic?
No. Alfuzosin is not on the DEA controlled substances list, so the DEA does not classify it as a narcotic. Its FDA established pharmacologic class is alpha-Adrenergic Blocker.
Does this page cover state schedules?
No. This page reports the federal schedule only. Some states schedule drugs on their own; check your state board of pharmacy.