NDC 62935-753 – Eligard

· Kit · Subcutaneous

Human Prescription Drug 1 recall

Product NDC62935-753

Product details

Brand name
Eligard
Generic name
Leuprolide Acetate
Labeler
TOLMAR Inc.
Dosage form
Kit
Route
Subcutaneous
Marketing category
NDA · NDA021343
Marketed since
May 15, 2002
Listing expires
December 31, 2026

Active ingredients

    Uses, dosage, side effects and warnings for Eligard →

    Package NDC codes (1)

    Package NDCDescriptionSince
    62935-753-751 KIT in 1 CARTON (62935-753-75) * .25 mL in 1 SYRINGE (62935-754-74) * .25 mL in 1 SYRINGE (62935-755-75)May 15, 2002

    Recalls mentioning this NDC

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