NDC 63629-9155 – Alfuzosin hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC63629-9155
Product details
- Brand name
- Alfuzosin hydrochloride
- Generic name
- Alfuzosin hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203192
- Marketed since
- March 15, 2016
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 63629-9155-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-1) | Apr 29, 2022 |
| 63629-9155-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-2) | Apr 29, 2022 |
| 63629-9155-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-3) | Apr 29, 2022 |
| 63629-9155-4 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-9155-4) | Apr 29, 2022 |
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