USFDA APPLICATION NUMBER - 21394 / DOSAGE - TABLET;ORAL - 38MG;200MG
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
DIPHENHYDRAMINE CITRATE(UNII: 4OD433S209) (DIPHENHYDRAMINE - UNII:8GTS82S83M) | DIPHENHYDRAMINE CITRATE | 38mg |
IBUPROFEN(UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 200mg |
Inactive Ingredients
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