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) |
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