USFDA APPLICATION NUMBER - 17876 / DOSAGE - TABLET;ORAL-21 - 0.02MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
ETHINYL ESTRADIOL(UNII: 423D2T571U) (ETHINYL ESTRADIOL - UNII:423D2T571U) | ETHINYL ESTRADIOL | 0.02mg | 0.03mg |
NORETHINDRONE ACETATE(UNII: 9S44LIC7OJ) (NORETHINDRONE - UNII:T18F433X4S) | NORETHINDRONE ACETATE | 1mg | 1.5mg |
Inactive Ingredients
Ingredient Name | Actavis Pharma, Inc. | Mayne Pharma Inc. |
---|---|---|
ACACIA(5C5403N26O) | ||
D&C YELLOW NO. 10(35SW5USQ3G) | ||
FD&C BLUE NO. 1(H3R47K3TBD) | ||
FD&C YELLOW NO. 6(H77VEI93A8) | ||
LACTOSE(J2B2A4N98G) | ||
LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | ||
MAGNESIUM STEARATE(70097M6I30) | ||
STARCH, CORN(O8232NY3SJ) | ||
SUCROSE(C151H8M554) | ||
SUGARCANE(81H2R5AOH3) | ||
TALC(7SEV7J4R1U) |
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