Alfuzosin Hydrochloride 51655-0967
Product NDC
51655-0967- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 29, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA203192
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Alfuzosin Hydrochloride | 10 mg/1 |
Drug Class
Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]
Packaging Options(1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)