USFDA APPLICATION NUMBER - 50808 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 135MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
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