all day pain relief - Naproxen sodium
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NDC Code: | 59779-061 |
Proprietary Name: | all day pain relief |
Suffix: | |
Non-Proprietary Name: | Naproxen sodium |
Dosage Form: | TABLET, FILM COATED |
Method: | ORAL |
Original Marketing Date: | 26-09-2005 |
Category Name: | ANDA |
Application Number: | ANDA074661 |
Labeler: | CVS PHARMACY |
Substance Name: | NAPROXEN SODIUM |
Active Numerator Strength: | 220 |
Active Ingredient Unit: | mg/1 |
Pharm Classes: | |
DEA Schedule: |