 
				 
										
USFDA APPLICATION NUMBER - 50582 / DOSAGE - CAPSULE, DELAYED RELEASE;ORAL - EQ 100MG BASE
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| DOXYCYCLINE HYCLATE(UNII: 19XTS3T51U) (DOXYCYCLINE ANHYDROUS - UNII:334895S862) | DOXYCYCLINE ANHYDROUS | 100mg | 75mg | 
Inactive Ingredients
| Ingredient Name | Allergan, Inc. | 
|---|---|
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
| D&C YELLOW NO. 10(35SW5USQ3G) | |
| FD&C BLUE NO. 1(H3R47K3TBD) | |
| FD&C YELLOW NO. 6(H77VEI93A8) | |
| GELATIN(2G86QN327L) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| POVIDONE(FZ989GH94E) | |
| SILICON DIOXIDE(ETJ7Z6XBU4) | |
| SODIUM LAURYL SULFATE(368GB5141J) | |
| STARCH, WHEAT(79QS2MG2LP) | |
| TITANIUM DIOXIDE(15FIX9V2JP) |