NDC 84386-153 – Alfuzosin Hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC84386-153
Product details
- Brand name
- Alfuzosin Hydrochloride
- Generic name
- Alfuzosin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079060
- Marketed since
- July 1, 2026
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 84386-153-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-01) | Jul 1, 2026 |
| 84386-153-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-05) | Jul 1, 2026 |
| 84386-153-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-30) | Jul 1, 2026 |
| 84386-153-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-90) | Jul 1, 2026 |
| 84386-153-99 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-99) | Jul 1, 2026 |
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