NDC 59651-021

Dutasteride 0.5 mg capsule, liquid filled

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Dutasteride: every company that makes it
Form
capsule, liquid filled, oral
Strength
0.5 mg
Approval
ANDA ANDA202660
On the market since
Jan 20, 2023
Package NDCs
59651-021-30 59651-021-90
Official label
DailyMed (National Library of Medicine), updated Sep 11, 2025

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