 
				 
										
USFDA APPLICATION NUMBER - 50795 / DOSAGE - TABLET, DELAYED RELEASE;ORAL - EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 75mg in 100 | 
Inactive Ingredients
| Ingredient Name | Allergan, Inc. | Mayne Pharma International Pty Ltd | 
|---|---|---|
| ANHYDROUS LACTOSE(3SY5LH9PMK) | ||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
| CROSPOVIDONE(2S7830E561) | ||
| CROSPOVIDONE(68401960MK) | ||
| LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||
| MAGNESIUM STEARATE(70097M6I30) | ||
| SODIUM CHLORIDE(451W47IQ8X) | ||
| SODIUM LAURYL SULFATE(368GB5141J) | ||
| STARCH, CORN(O8232NY3SJ) | ||
| TALC(7SEV7J4R1U) |