Tamsulosin Hydrochloride 00781-2076
Product NDC
00781-2076- Manufacturer
- Sandoz Inc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 27, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA078015
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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(3)
100 CAPSULE in 1 BOTTLE (0781-2076-01)
1000 CAPSULE in 1 BOTTLE (0781-2076-10)
90 CAPSULE in 1 BOTTLE (0781-2076-92)