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norelgestromin and ethinyl estradiol

NDC 70710-1190 · Zydus Pharmaceuticals USA Inc.

Generic namenorelgestromin and ethinyl estradiol
Dosage formPATCH
RouteTRANSDERMAL
Active ingredient(s)NORELGESTROMIN, ETHINYL ESTRADIOL
Strength35; 150 ug/mg; ug/mg
Pharmacologic classEstrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC]
Marketing categoryANDA

Packages

70710-1190-3 — 3 POUCH in 1 CARTON (70710-1190-3) / 1 POUCH in 1 POUCH (70710-1190-1) / 7 mg in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-827 — Norethindrone Acetate and Ethinyl Estradiol, 68180-828 — Norethindrone Acetate and Ethinyl Estradiol, 68308-752 — segesterone acetate and ethinyl estradiol, 68462-132 — Norethindrone Acetate and Ethinyl Estradiol, 68462-504 — Norethindrone Acetate and Ethinyl Estradiol, 68462-637 — Levonorgestrel and Ethinyl Estradiol, 68462-656 — Norethindrone Acetate and Ethinyl Estradiol, 68462-657 — Norethindrone Acetate and Ethinyl Estradiol, 69238-1521 — Norelgestromin and Ethinly Estradiol, 70700-156 — Etonogestrel and Ethinyl Estradiol Vaginal, 70700-313 — norethindrone acetate and ethinyl estradiol, 70700-314 — norethindrone acetate and ethinyl estradiol, 70771-1777 — norelgestromin and ethinyl estradiol, 71671-100 — levonorgestrel/ethinyl estradiol, 72162-2220 — Norelgestromin and Ethinyl Estradiol, 72189-215 — Junel FE, 75834-129 — Norethindrone Acetate and Ethinyl Estradiol, 75834-130 — Norethindrone Acetate and Ethinyl Estradiol, 78206-146 — etonogestrel and ethinyl estradiol, 82804-172 — Norethindrone Acetate and Ethinyl Estradiol, +27 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.