NDC 50742-658 – Estradiol and Norethindrone Acetate

Estradiol .5 mg/1; Norethindrone Acetate .1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50742-658

Product details

Brand name
Estradiol and Norethindrone Acetate
Generic name
Estradiol and Norethindrone Acetate
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210612
Marketed since
April 3, 2019
Listing expires
December 31, 2027
Pharmacologic class
Estrogen; Progestin

Active ingredients

Uses, dosage, side effects and warnings for Estradiol and Norethindrone Acetate →

Package NDC codes (3)

Package NDCDescriptionSince
50742-658-281 BLISTER PACK in 1 CARTON (50742-658-28) / 28 TABLET in 1 BLISTER PACKApr 3, 2019
50742-658-686 BLISTER PACK in 1 CARTON (50742-658-68) / 28 TABLET in 1 BLISTER PACKApr 3, 2019
50742-658-843 BLISTER PACK in 1 CARTON (50742-658-84) / 28 TABLET in 1 BLISTER PACKApr 3, 2019

Other Estradiol and Norethindrone Acetate products