NDC 51991-623 – Estradiol / Norethindrone Acetate

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

Human Prescription Drug

Product NDC51991-623

Product details

Brand name
Estradiol / Norethindrone Acetate
Generic name
Estradiol and Norethindrone Acetate
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078324
Marketed since
June 9, 2011
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Progestin

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
51991-623-281 BLISTER PACK in 1 CARTON (51991-623-28) / 28 TABLET, FILM COATED in 1 BLISTER PACKJun 9, 2011

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