
USFDA APPLICATION NUMBER - 50007 / DOSAGE - CAPSULE;ORAL - EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| DOXYCYCLINE HYCLATE(UNII: 19XTS3T51U) (DOXYCYCLINE ANHYDROUS - UNII:334895S862) | DOXYCYCLINE ANHYDROUS | 100mg |
Inactive Ingredients
| Ingredient Name | Greenstone LLC |
|---|---|
| FD&C BLUE NO. 1(H3R47K3TBD) | |
| GELATIN, UNSPECIFIED(2G86QN327L) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| SODIUM LAURYL SULFATE(368GB5141J) |