Prazosin Hydrochloride 70518-2178
Product NDC
70518-2178- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA210971
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prazosin Hydrochloride | 2 mg/1 |
Drug Class
Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]
Packaging Options(1)
100 POUCH in 1 BOX (70518-2178-2) / 1 CAPSULE in 1 POUCH (70518-2178-3)