Tamsulosin Hydrochloride 72603-0115
Product NDC
72603-0115- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 30, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA202433
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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(2)
100 CAPSULE in 1 BOTTLE (72603-115-01)
500 CAPSULE in 1 BOTTLE (72603-115-02)