Product NDC: | 54569-0235 |
Proprietary Name: | Allopurinol |
Non Proprietary Name: | allopurinol |
Active Ingredient(s): | 300 mg/1 & nbsp; allopurinol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-0235 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075798 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030627 |
Package NDC: | 54569-0235-0 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (54569-0235-0) |
NDC Code | 54569-0235-0 |
Proprietary Name | Allopurinol |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (54569-0235-0) |
Product NDC | 54569-0235 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | allopurinol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20030627 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | ALLOPURINOL |
Strength Number | 300 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |