Lyleq

NDC 50102-300 · Afaxys Pharma, LLC

Generic nameNORETHINDRONE

Dosage formTABLET

RouteORAL

Active ingredient(s)NORETHINDRONE

Strength.35 mg/1

Pharmacologic classProgesterone Congeners [CS], Progestin [EPC]

Marketing categoryANDA

Packages

50102-300-13 — 3 PACKAGE in 1 CARTON (50102-300-13) / 1 BLISTER PACK in 1 PACKAGE (50102-300-11) / 28 TABLET in 1 BLISTER PACK (50102-300-01)

FDA lists these products with the same active ingredient.

0378-7292 — norethindrone, 0480-3475 — Norethindrone, 0555-9009 — Norethindrone and Ethinyl Estradiol, 50090-6161 — NORETHINDRONE, 51862-884 — NORETHINDRONE, 51862-886 — NORETHINDRONE, 59651-136 — NORETHINDRONE, 63187-748 — Norethindrone, 65862-925 — NORETHINDRONE, 68180-876 — NORETHINDRONE, 68180-877 — norethindrone, 68462-303 — Norethindrone, 68462-305 — Norethindrone, 70700-316 — norethindrone, 70700-317 — Norethindrone, 71205-526 — NORETHINDRONE, 75907-074 — NORETHINDRONE, 75907-075 — NORETHINDRONE, 79929-015 — Norethindrone, 82804-175 — NORETHINDRONE

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