NDC 42023-259

Leuprolide Acetate 1 mg per 0.2 mL injection

On the label: ENDO USA, 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 ENDO USA, Inc. names for other drugs.

Product details

Generic drug
Leuprolide: every company that makes it
Form
injection, subcutaneous
Strength
1 mg per 0.2 mL
Approval
ANDA ANDA217437
On the market since
Jun 30, 2026
Package NDCs
42023-259-00 42023-259-01
Official label
DailyMed (National Library of Medicine), updated Jun 10, 2024

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