NDC 62935-753

Eligard 7.5 mg per 0.25 mL kit

On the label: TOLMAR Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants TOLMAR Inc. names for other drugs.

Recalls

Sep 12, 2023 · Class III · Tolmar, Inc.
Superpotent Drug - Higher than expected levels of leuprolide acetate in the constituted product.
Lots: Lot: 13635A1, Exp. 07/31/2024

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug: Leuprolide: every company that makes it
Form: kit, subcutaneous
Strength: 7.5 mg per 0.25 mL
Approval: NDA NDA021343
On the market since: May 15, 2002
Package NDCs: 62935-753-75 62935-754-74 62935-755-75
Official label: DailyMed (National Library of Medicine), updated Apr 29, 2019

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