NDC 65862-249 – Alfuzosin Hydrochloride
Alfuzosin Hydrochloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC65862-249
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
- August 30, 2012
- 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 |
|---|---|---|
| 65862-249-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01) | Aug 30, 2012 |
| 65862-249-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-05) | Aug 30, 2012 |
| 65862-249-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-30) | Aug 30, 2012 |
| 65862-249-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-90) | Aug 30, 2012 |
| 65862-249-99 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-99) | Aug 30, 2012 |
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