All Day Pain Relief - Naproxen Sodium
Navigation: NDC > Supplier starting with: E > EQUALINE (SUPERVALU)| Field | Value |
|---|---|
| NDC Code: | 41163-167 |
| Proprietary Name: | All Day Pain Relief |
| Suffix: | |
| Non-Proprietary Name: | Naproxen Sodium |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 09-05-2013 |
| Category Name: | ANDA |
| Application Number: | ANDA079096 |
| Labeler: | EQUALINE (SUPERVALU) |
| Substance Name: | NAPROXEN SODIUM |
| Active Numerator Strength: | 220 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |