NDC 0143-9533
Allopurinol sodium
Allopurinol Sodium
Allopurinol sodium is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Hikma Pharmaceuticals Usa Inc.. The primary component is Allopurinol Sodium.
Product ID | 0143-9533_0083505e-a473-4236-ac5d-c892d0c05158 |
NDC | 0143-9533 |
Product Type | Human Prescription Drug |
Proprietary Name | Allopurinol sodium |
Generic Name | Allopurinol Sodium |
Dosage Form | Injection, Powder, Lyophilized, For Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2004-09-01 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076870 |
Labeler Name | Hikma Pharmaceuticals USA Inc. |
Substance Name | ALLOPURINOL SODIUM |
Active Ingredient Strength | 500 mg/25mL |
Pharm Classes | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |