Allopurinol - Allopurinol
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-5543 |
| Proprietary Name: | Allopurinol |
| Suffix: | |
| Non-Proprietary Name: | Allopurinol |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 06-04-2009 |
| Category Name: | NDA |
| Application Number: | NDA018832 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | ALLOPURINOL |
| Active Numerator Strength: | 100 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
| DEA Schedule: |