NDC 70700-116 – Altavera

· Kit

Human Prescription Drug 1 recall

Product NDC70700-116

Product details

Brand name
Altavera
Generic name
Levonorgestrel and Ethinyl Estradiol
Labeler
Xiromed, LLC.
Dosage form
Kit
Marketing category
ANDA · ANDA079102
Marketed since
September 1, 2022
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Altavera →

    Package NDC codes (1)

    Package NDCDescriptionSince
    70700-116-853 BLISTER PACK in 1 CARTON (70700-116-85) / 1 KIT in 1 BLISTER PACKMar 2, 2023

    Recalls mentioning this NDC

    Other Altavera products