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LOPREEZA

NDC 69238-1610 · Amneal Pharmaceuticals NY LLC

Generic nameestradiol/norethindrone acetate
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ESTRADIOL, NORETHINDRONE ACETATE
Strength1; .5 mg/1; mg/1
Pharmacologic classEstradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC]
Marketing categoryNDA

Packages

69238-1610-6 — 1 BLISTER PACK in 1 CARTON (69238-1610-6) / 28 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68968-6650 — estradiol, 68968-6675 — estradiol, 69238-1251 — estradiol/norethindrone acetate, 69238-1252 — estradiol/norethindrone acetate, 69238-1293 — Estradiol, 69238-1294 — Estradiol, 69238-1295 — Estradiol, 69238-1296 — Estradiol, 69238-1447 — Estradiol, 69238-1609 — estradiol/norethindrone acetate, 69238-1629 — Estradiol, 69238-1630 — Estradiol, 69238-1631 — Estradiol, 69238-1632 — Estradiol, 69238-1633 — Estradiol, 69238-2448 — Estradiol Transdermal, 69238-2449 — Estradiol Transdermal, 69238-2450 — Estradiol Transdermal, 69238-2451 — Estradiol Transdermal, 69238-2452 — Estradiol Transdermal, +289 more

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