NDC 70954-019 – Prazosin Hydrochloride
Prazosin Hydrochloride 1 mg/1 · Capsule · Oral
Product NDC70954-019
Product details
- Brand name
- Prazosin Hydrochloride
- Generic name
- Prazosin Hydrochloride
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA210971
- Marketed since
- October 3, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Prazosin Hydrochloride 1 mg/1
Uses, dosage, side effects and warnings for Prazosin Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70954-019-10 | 100 CAPSULE in 1 BOTTLE (70954-019-10) | Oct 3, 2018 |
| 70954-019-20 | 1000 CAPSULE in 1 BOTTLE (70954-019-20) | Oct 3, 2018 |
| 70954-019-40 | 100 BLISTER PACK in 1 CARTON (70954-019-40) / 1 CAPSULE in 1 BLISTER PACK (70954-019-30) | Apr 13, 2021 |
| 70954-019-50 | 90 CAPSULE in 1 BOTTLE (70954-019-50) | Sep 7, 2021 |
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