NDC 51655-087 – Alfuzosin Hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC51655-087
Product details
- Brand name
- Alfuzosin Hydrochloride
- Generic name
- Alfuzosin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079060
- Marketed since
- October 4, 2022
- 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 |
|---|---|---|
| 51655-087-52 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52) | Oct 4, 2022 |
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