NDC 55566-7501 – Menopur

· Kit

Human Prescription Drug 1 recall

Product NDC55566-7501

Product details

Brand name
Menopur
Generic name
Menotropins
Labeler
Ferring Pharmaceuticals Inc.
Dosage form
Kit
Marketing category
BLA · BLA021663
Marketed since
October 29, 2004
Listing expires
December 31, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Menopur →

    Package NDC codes (1)

    Package NDCDescriptionSince
    55566-7501-21 CARTON in 1 CARTON (55566-7501-2) / 1 KIT in 1 CARTON (55566-7501-1) * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55566-7502-0) * 1 INJECTION in 1 VIAL (55566-1600-0)Oct 29, 2004

    Recalls mentioning this NDC