All Day Pain Relief - Naproxen Sodium
Navigation: NDC > Supplier starting with: H > H E B| Field | Value |
|---|---|
| NDC Code: | 37808-500 |
| Proprietary Name: | All Day Pain Relief |
| Suffix: | |
| Non-Proprietary Name: | Naproxen Sodium |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 24-02-1997 |
| Category Name: | ANDA |
| Application Number: | ANDA074661 |
| Labeler: | H E B |
| Substance Name: | NAPROXEN SODIUM |
| Active Numerator Strength: | 220 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | |
| DEA Schedule: |