NDC 71335-1724 – Prazosin Hydrochloride
Prazosin Hydrochloride 1 mg/1 · Capsule · Oral
Product NDC71335-1724
Product details
- Brand name
- Prazosin Hydrochloride
- Generic name
- Prazosin hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA072575
- Marketed since
- February 28, 1989
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Prazosin Hydrochloride 1 mg/1
Uses, dosage, side effects and warnings for Prazosin Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1724-1 | 30 CAPSULE in 1 BOTTLE (71335-1724-1) | Nov 25, 2020 |
| 71335-1724-2 | 100 CAPSULE in 1 BOTTLE (71335-1724-2) | Jul 1, 2022 |
| 71335-1724-3 | 60 CAPSULE in 1 BOTTLE (71335-1724-3) | Jan 12, 2021 |
| 71335-1724-4 | 28 CAPSULE in 1 BOTTLE (71335-1724-4) | Jul 1, 2022 |
| 71335-1724-5 | 90 CAPSULE in 1 BOTTLE (71335-1724-5) | Jul 1, 2022 |
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