NDC 69238-1609 – Lopreeza

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

Human Prescription Drug

Product NDC69238-1609

Product details

Brand name
Lopreeza
Generic name
Estradiol/norethindrone acetate
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA020907
Marketed since
January 7, 2019
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Progestin

Active ingredients

Uses, dosage, side effects and warnings for Lopreeza →

Package NDC codes (1)

Package NDCDescriptionSince
69238-1609-61 BLISTER PACK in 1 CARTON (69238-1609-6) / 28 TABLET, FILM COATED in 1 BLISTER PACKJan 7, 2019

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