NDC 0143-9533 – Allopurinol sodium
Allopurinol Sodium 500 mg/25mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC0143-9533
Product details
- Brand name
- Allopurinol sodium
- Generic name
- Allopurinol sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA076870
- Marketed since
- September 1, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol Sodium 500 mg/25mL
Uses, dosage, side effects and warnings for Allopurinol sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9533-01 | 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) / 25 mL in 1 VIAL | Sep 1, 2004 |