Alfuzosin Hydrochloride 29300-0155
Product NDC
29300-0155- Manufacturer
- Unichem Pharmaceuticals (usa), Inc.
- 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(3)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-01)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-13)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-19)