NDC 51285-127 – Loestrin 21 Day

Norethindrone Acetate 1.5 mg/1; Ethinyl Estradiol 30 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC51285-127

Product details

Brand name
Loestrin 21 Day
Generic name
Norethindrone Acetate and Ethinyl Estradiol
Labeler
Teva Women's Health LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076381
Marketed since
February 26, 2015
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Progestin

Active ingredients

Uses, dosage, side effects and warnings for Loestrin →

Package NDC codes (1)

Package NDCDescriptionSince
51285-127-975 POUCH in 1 CARTON (51285-127-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACKFeb 26, 2015

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