NDC 51655-087-52
Alfuzosin Hydrochloride 10 mg/1
Alfuzosin Hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Alfuzosin Hydrochloride is a tablet, film coated, extended release containing alfuzosin hydrochloride at a strength of 10 mg/1. Manufactured by Northwind Health Company, LLC.
Key Facts
- Brand Name
- Alfuzosin Hydrochloride
- Generic Name
- Alfuzosin Hydrochloride
- NDC Code (Package)
51655-087-52- NDC Code (Product)
51655-087- Manufacturer
- Northwind Health Company, LLC
- Strength
- 10 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079060
- Marketing Start
- 10/04/2022
Recall History
No Recall HistoryView Full Drug Page
Alfuzosin Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.