NDC 68180-857 – Levonorgestrel and Ethinyl Estradiol

· Kit

Human Prescription Drug 1 recall

Product NDC68180-857

Product details

Brand name
Levonorgestrel and Ethinyl Estradiol
Generic name
Levonorgestrel and Ethinyl Estradiol
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Kit
Marketing category
ANDA · ANDA200248
Marketed since
August 30, 2020
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Levonorgestrel and ethinyl estradiol →

    Package NDC codes (1)

    Package NDCDescriptionSince
    68180-857-733 CARTON in 1 CARTON (68180-857-73) / 1 KIT in 1 CARTONAug 30, 2020

    Recalls mentioning this NDC

    Other Levonorgestrel and ethinyl estradiol products