NDC 76282-302 – Alfuzosin hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC76282-302
Product details
- Brand name
- Alfuzosin hydrochloride
- Generic name
- Alfuzosin hydrochloride
- Labeler
- Exelan Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090284
- Marketed since
- October 2, 2012
- 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 |
|---|---|---|
| 76282-302-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01) | Oct 2, 2012 |
| 76282-302-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-05) | Oct 2, 2012 |
| 76282-302-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-10) | Oct 2, 2012 |
| 76282-302-12 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-12) | Dec 1, 2022 |
| 76282-302-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-90) | Jan 1, 2019 |
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