NDC 0378-7280 – Norethindrone Acetate And Ethinyl Estradiol

Ethinyl Estradiol .02 mg/1; Norethindrone Acetate 1 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0378-7280

Product details

Brand name
Norethindrone Acetate And Ethinyl Estradiol
Generic name
norethindrone acetate and ethinyl estradiol
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202771
Marketed since
July 11, 2014
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Progestin

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0378-7280-533 POUCH in 1 CARTON (0378-7280-53) / 1 BLISTER PACK in 1 POUCH (0378-7280-85) / 21 TABLET in 1 BLISTER PACKNov 7, 2014

Recalls mentioning this NDC

Other Norethindrone Acetate and Ethinyl Estradiol products