Prazosin Hydrochloride 70518-3679
Product NDC
70518-3679- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 12, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA215697
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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)
30 CAPSULE in 1 BLISTER PACK (70518-3679-0)