NDC 0093-4068 – Prazosin Hydrochloride
Prazosin Hydrochloride 2 mg/1 · Capsule · Oral
Product NDC0093-4068
Product details
- Brand name
- Prazosin Hydrochloride
- Generic name
- Prazosin Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA071745
- Marketed since
- February 22, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Prazosin Hydrochloride 2 mg/1
Uses, dosage, side effects and warnings for Prazosin Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-4068-01 | 100 CAPSULE in 1 BOTTLE (0093-4068-01) | Feb 22, 2007 |
| 0093-4068-10 | 1000 CAPSULE in 1 BOTTLE (0093-4068-10) | Feb 22, 2007 |
Recalls mentioning this NDC
- D-0105-2026 Nov 5, 2025 · Class II
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots. - D-0104-2026 Nov 5, 2025 · Class II
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots. - D-0106-2026 Nov 5, 2025 · Class II
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
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