
USFDA APPLICATION NUMBER - 20067 / DOSAGE - TABLET, DELAYED RELEASE;ORAL - 500MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| naproxen sodium(UNII: 9TN87S3A3C) (naproxen - UNII:57Y76R9ATQ) | naproxen sodium | 550mg |
| naproxen(UNII: 57Y76R9ATQ) (naproxen - UNII:57Y76R9ATQ) | naproxen | 500mg | 375mg | 500mg |
Inactive Ingredients