NDC 60687-572 – Prazosin Hydrochloride
Prazosin Hydrochloride 5 mg/1 · Capsule · Oral
Product NDC60687-572
Product details
- Brand name
- Prazosin Hydrochloride
- Generic name
- Prazosin Hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA071745
- Marketed since
- April 21, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Prazosin Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Prazosin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-572-32 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-572-32) / 1 CAPSULE in 1 BLISTER PACK (60687-572-33) | Apr 21, 2021 |
Recalls mentioning this NDC
- D-0103-2026 Nov 5, 2025 · Class II
Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit
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