
USFDA APPLICATION NUMBER - 50808 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 115MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| minocycline hydrochloride(UNII: 0020414E5U) (minocycline - UNII:FYY3R43WGO) | minocycline | 105mg | 80mg | 55mg |
Inactive Ingredients
| Ingredient Name | Oceanside Pharmaceuticals |
|---|---|
| CARNAUBA WAX(R12CBM0EIZ) | |
| D&C Red No. 27(2LRS185U6K) | |
| FD&C Blue No. 1(H3R47K3TBD) | |
| FD&C Blue No. 2(L06K8R7DQK) | |
| FD&C RED NO. 40(WZB9127XOA) | |
| FD&C Yellow No. 6(H77VEI93A8) | |
| HYPROMELLOSE 2910 (50 MPA.S)(1IVH67816N) | |
| LACTOSE MONOHYDRATE(EWQ57Q8I5X) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| POLYETHYLENE GLYCOL 3350(G2M7P15E5P) | |
| SILICON DIOXIDE(ETJ7Z6XBU4) | |
| TITANIUM DIOXIDE(15FIX9V2JP) | |
| TRIACETIN(XHX3C3X673) |