Home
>
National Drug Code (NDC)
>
ZYLOPRIM
ZYLOPRIM - 65483-991-10 - (allopurinol)
Drug Information of ZYLOPRIM
| Product NDC: | 65483-991 |
| Proprietary Name: | ZYLOPRIM |
| Non Proprietary Name: | allopurinol |
| Active Ingredient(s): | 100 mg/1 & nbsp; allopurinol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZYLOPRIM
| Product NDC: | 65483-991 |
| Labeler Name: | Prometheus Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016084 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19660819 |
Package Information of ZYLOPRIM
| Package NDC: | 65483-991-10 |
| Package Description: | 100 TABLET in 1 BOTTLE (65483-991-10) |
NDC Information of ZYLOPRIM
| NDC Code | 65483-991-10 |
| Proprietary Name | ZYLOPRIM |
| Package Description | 100 TABLET in 1 BOTTLE (65483-991-10) |
| Product NDC | 65483-991 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | allopurinol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19660819 |
| Marketing Category Name | NDA |
| Labeler Name | Prometheus Laboratories Inc. |
| Substance Name | ALLOPURINOL |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
