NDC 0555-9027 – Junel 21 Day

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

Human Prescription Drug 1 recall

Product NDC0555-9027

Product details

Brand name
Junel 21 Day
Generic name
Norethindrone Acetate and Ethinyl Estradiol
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076381
Marketed since
September 18, 2003
Listing expires
December 31, 2026
Pharmacologic class
Estrogen; Progestin

Active ingredients

Uses, dosage, side effects and warnings for Junel →

Package NDC codes (1)

Package NDCDescriptionSince
0555-9027-423 POUCH in 1 CARTON (0555-9027-42) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACKSep 18, 2003

Recalls mentioning this NDC

Other Junel products