NDC 0378-2302 – Prazosin Hydrochloride
Prazosin Hydrochloride 2 mg/1 · Capsule · Oral
Product NDC0378-2302
Product details
- Brand name
- Prazosin Hydrochloride
- Generic name
- Prazosin hydrochloride
- Labeler
- Mylan Pharmaceuticals Inc.
- 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 2 mg/1
Uses, dosage, side effects and warnings for Prazosin Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0378-2302-01 | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-01) | Feb 28, 1989 |
| 0378-2302-10 | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0378-2302-10) | Feb 28, 1989 |
Recalls mentioning this NDC
- D-1093-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse
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