NDC 69097-844 – Alfuzosin Hydrochloride extended release
Alfuzosin Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC69097-844
Product details
- Brand name
- Alfuzosin Hydrochloride extended release
- Generic name
- Alfuzosin Hydrochloride
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090284
- Marketed since
- June 30, 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 |
|---|---|---|
| 69097-844-02 | 30 TABLET in 1 BOTTLE (69097-844-02) | Jun 30, 2016 |
| 69097-844-05 | 90 TABLET in 1 BOTTLE (69097-844-05) | Jun 30, 2016 |
| 69097-844-07 | 100 TABLET in 1 BOTTLE (69097-844-07) | Jun 30, 2016 |
| 69097-844-12 | 500 TABLET in 1 BOTTLE (69097-844-12) | Jun 30, 2016 |
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