Norethindrone Acetate

NDC 68462-304 · Glenmark Pharmaceuticals Inc., USA

Generic nameNorethindrone Acetate

Dosage formTABLET

RouteORAL

Active ingredient(s)NORETHINDRONE ACETATE

Strength5 mg/1

Pharmacologic classProgesterone Congeners [CS], Progestin [EPC]

Marketing categoryANDA

Packages

68462-304-05 — 500 TABLET in 1 BOTTLE (68462-304-05)

68462-304-50 — 50 TABLET in 1 BOTTLE (68462-304-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-425 — ESTRADIOL AND NORETHINDRONE ACETATE, 60687-921 — Norethindrone Acetate, 60846-231 — Estradiol/norethindrone acetate, 60846-232 — Estradiol/norethindrone acetate, 65162-475 — Norethindrone, 65862-935 — Norethindrone Acetate and Ethinyl Estradiol, 65862-939 — Norethindrone Acetate and Ethinyl Estradiol, 68180-827 — Norethindrone Acetate and Ethinyl Estradiol, 68180-828 — Norethindrone Acetate and Ethinyl Estradiol, 68462-132 — Norethindrone Acetate and Ethinyl Estradiol, 68462-504 — Norethindrone Acetate and Ethinyl Estradiol, 68462-656 — Norethindrone Acetate and Ethinyl Estradiol, 68462-657 — Norethindrone Acetate and Ethinyl Estradiol, 68968-0514 — estradiol/norethindrone acetate transdermal system, 68968-0525 — estradiol/norethindrone acetate transdermal system, 69238-1251 — estradiol/norethindrone acetate, 69238-1252 — estradiol/norethindrone acetate, 69238-1609 — estradiol/norethindrone acetate, 69238-1610 — estradiol/norethindrone acetate, 70700-303 — estradiol and norethindrone acetate, +30 more

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