
USFDA APPLICATION NUMBER - 20972 / DOSAGE - CAPSULE;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |