oxaprozin - OXAPROZIN
Navigation: NDC > Supplier starting with: G > GREENSTONE LLC| Field | Value |
|---|---|
| NDC Code: | 59762-6002 |
| Proprietary Name: | oxaprozin |
| Suffix: | |
| Non-Proprietary Name: | OXAPROZIN |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 28-03-2013 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA018841 |
| Labeler: | GREENSTONE LLC |
| Substance Name: | OXAPROZIN |
| Active Numerator Strength: | 600 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: |