Tamsulosin Hydrochloride 82009-0025
Product NDC
82009-0025- Manufacturer
- Quallent Pharmaceuticals Health Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 20, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA078225
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tamsulosin Hydrochloride | .4 mg/1 |
Drug Class
Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]
Packaging Options(1)
1000 CAPSULE in 1 BOTTLE (82009-025-10)