Prazosin Hydrochloride 00378-2302
Product NDC
00378-2302- Manufacturer
- Mylan Pharmaceuticals Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 28, 1989
- Listing Expires
- December 31, 2026
- Application
- ANDA072575
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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(2)
100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-01)
1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-10)