NDC 51862-890 – Azurette

· Kit

Human Prescription Drug

Product NDC51862-890

Product details

Brand name
Azurette
Generic name
Desogestrel/ethinyl estradiol and ethinyl estradiol
Labeler
Mayne Pharma Inc.
Dosage form
Kit
Marketing category
ANDA · ANDA091247
Marketed since
October 3, 2020
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Azurette →

    Package NDC codes (3)

    Package NDCDescriptionSince
    51862-890-011 BLISTER PACK in 1 PACKET (51862-890-01) / 1 KIT in 1 BLISTER PACKOct 3, 2020
    51862-890-021 BLISTER PACK in 1 CARTON (51862-890-02) / 1 KIT in 1 BLISTER PACKOct 3, 2020
    51862-890-033 BLISTER PACK in 1 CARTON (51862-890-03) / 1 KIT in 1 BLISTER PACKOct 3, 2020

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