NDC 70377-068 – Prazosin hydrochloride
Prazosin Hydrochloride 5 mg/1 · Capsule · Oral
Product NDC70377-068
Product details
- Brand name
- Prazosin hydrochloride
- Generic name
- Prazosin hydrochloride
- Labeler
- Biocon Pharma Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA213406
- Marketed since
- January 9, 2023
- 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 |
|---|---|---|
| 70377-068-11 | 100 CAPSULE in 1 BOTTLE (70377-068-11) | Jan 9, 2023 |
Recalls mentioning this NDC
- D-0419-2026 Apr 8, 2026 · Class II
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits. - D-0420-2026 Apr 8, 2026 · Class II
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits. - D-0421-2026 Apr 8, 2026 · Class II
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
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