NDC 72162-1449 – Alfuzosin Hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC72162-1449
Product details
- Brand name
- Alfuzosin Hydrochloride
- Generic name
- Alfuzosin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079057
- Marketed since
- November 22, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Alfuzosin Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Alfuzosin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1449-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1449-9) | Jul 16, 2024 |
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