NDC 70710-1769 – Leuprolide Acetate

· Kit

Human Prescription Drug

Product NDC70710-1769

Product details

Brand name
Leuprolide Acetate
Generic name
Leuprolide Acetate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Kit
Marketing category
ANDA · ANDA215826
Marketed since
January 8, 2026
Listing expires
December 31, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Leuprolide Acetate →

    Package NDC codes (1)

    Package NDCDescriptionSince
    70710-1769-31 KIT in 1 CARTON (70710-1769-3) * 1 VIAL, MULTI-DOSE in 1 CARTON (70710-1768-1) / 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET (70710-1897-8)Jan 8, 2026

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