NDC 72843-591

leuprolide acetate 5 mg per 1 mL / 0.7 mL per 1 mL kit

On the label: UBI Pharma Inc..

Taiwan: 1

Where it's made

FactoryWhereRoleLast FDA inspection
UBI Pharma Inc.Hukou, TaiwanMakes it Problems found, fixed voluntarilyJun 6, 2023 · 4 inspections

Product details

Generic drug
Isopropyl Alcohol and Leuprolide: every company that makes it
Form
kit, subcutaneous
Strength
5 mg per 1 mL / 0.7 mL per 1 mL
Approval
ANDA ANDA217957
On the market since
Oct 25, 2024
Package NDCs
72843-590-01 72843-591-99
Official label
DailyMed (National Library of Medicine), updated Mar 29, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?