NDC 71288-558 – Cetrorelix Acetate

· Kit · Subcutaneous

Human Prescription Drug 1 recall

Product NDC71288-558

Product details

Brand name
Cetrorelix Acetate
Generic name
Cetrorelix Acetate
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
Kit
Route
Subcutaneous
Marketing category
ANDA · ANDA214540
Marketed since
April 24, 2024
Marketing end
April 30, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Cetrorelix acetate →

    Package NDC codes (1)

    Package NDCDescriptionSince
    71288-558-901 KIT in 1 CARTON (71288-558-90) * 2 mL in 1 VIAL, SINGLE-DOSE (71288-556-02) * 1 mL in 1 SYRINGE, GLASS (71288-557-81)Apr 24, 2024

    Recalls mentioning this NDC

    Other Cetrorelix acetate products