USFDA APPLICATION NUMBER - 20972 / DOSAGE - CAPSULE;ORAL - 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
EFAVIRENZ(UNII: JE6H2O27P8) (EFAVIRENZ - UNII:JE6H2O27P8) | EFAVIRENZ | 50mg | 200mg |
Inactive Ingredients
Ingredient Name | Aesica Queenborough Limited |
---|---|
LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |
MAGNESIUM STEARATE(70097M6I30) | |
SODIUM LAURYL SULFATE(368GB5141J) | |
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) |
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