NDC 47335-956 – Alfuzosin Hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC47335-956
Product details
- Brand name
- Alfuzosin Hydrochloride
- Generic name
- Alfuzosin Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 47335-956-08 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08) | Nov 22, 2011 |
| 47335-956-18 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18) | Nov 22, 2011 |
| 47335-956-81 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-81) | Nov 22, 2011 |
| 47335-956-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-83) | Nov 22, 2011 |
| 47335-956-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-88) | Nov 22, 2011 |
Recalls mentioning this NDC
- D-0502-2017 Mar 8, 2017 · Class II
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
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