NDC 50102-220 – Aubra EQ

· Kit

Human Prescription Drug

Product NDC50102-220

Product details

Brand name
Aubra EQ
Generic name
Levonorgestrel and Ethinyl Estradiol
Labeler
Afaxys Pharma, LLC
Dosage form
Kit
Marketing category
ANDA · ANDA206886
Marketed since
November 14, 2016
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Aubra EQ →

    Package NDC codes (1)

    Package NDCDescriptionSince
    50102-220-233 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACKNov 14, 2016

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