NDC 51655-967 – Alfuzosin hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Extended Release · Oral
Product NDC51655-967
Product details
- Brand name
- Alfuzosin hydrochloride
- Generic name
- Alfuzosin hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203192
- Marketed since
- June 29, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51655-967-52 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52) | Jun 29, 2023 |
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