Alfuzosin Hydrochloride 63629-9155
Product NDC
63629-9155- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 15, 2016
- Listing Expires
- December 31, 2026
- 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(4)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-1)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-2)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-3)
120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-4)