Allopurinol - allopurinol
Navigation: NDC > Supplier starting with: Q > QUALITEST PHARMACEUTICALS| Field | Value |
|---|---|
| NDC Code: | 0603-2115 |
| Proprietary Name: | Allopurinol |
| Suffix: | |
| Non-Proprietary Name: | allopurinol |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 27-06-2003 |
| Category Name: | ANDA |
| Application Number: | ANDA075798 |
| Labeler: | QUALITEST PHARMACEUTICALS |
| Substance Name: | ALLOPURINOL |
| Active Numerator Strength: | 100 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
| DEA Schedule: |