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Allopurinol sodium
Allopurinol sodium - 55390-106-01 - (Allopurinol sodium)
Drug Information of Allopurinol sodium
| Product NDC: | 55390-106 |
| Proprietary Name: | Allopurinol sodium |
| Non Proprietary Name: | Allopurinol sodium |
| Active Ingredient(s): | 500 mg/25mL & nbsp; Allopurinol sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allopurinol sodium
| Product NDC: | 55390-106 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076870 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040901 |
Package Information of Allopurinol sodium
| Package NDC: | 55390-106-01 |
| Package Description: | 1 VIAL in 1 BOX, UNIT-DOSE (55390-106-01) > 25 mL in 1 VIAL |
NDC Information of Allopurinol sodium
| NDC Code | 55390-106-01 |
| Proprietary Name | Allopurinol sodium |
| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-106-01) > 25 mL in 1 VIAL |
| Product NDC | 55390-106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Allopurinol sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20040901 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | ALLOPURINOL SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/25mL |
| Pharmaceutical Classes | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
