USFDA APPLICATION NUMBER - 22104 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 225MG BASE
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
VENLAFAXINE HYDROCHLORIDE(UNII: 7D7RX5A8MO) (VENLAFAXINE - UNII:GRZ5RCB1QG) | VENLAFAXINE | 75mg |
Inactive Ingredients
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