Tamsulosin Hydrochloride 61919-0703
Product NDC
61919-0703- Manufacturer
- Direct_rx
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 17, 2019
- Listing Expires
- December 31, 2027
- 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(1)
30 CAPSULE in 1 BOTTLE (61919-703-30)