NDC 65862-686

Finasteride 1 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

Where it's made

Aurobindo Pharma Limited

Medchal, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.

Product details

Generic drug
Finasteride: see every company that makes it
Form
tablet, film coated
Strength
1 mg
Approval
ANDA ANDA203687
On the market since
Nov 5, 2013
Package NDCs
65862-686-30 65862-686-90 65862-686-99
Official label
DailyMed (National Library of Medicine), updated Apr 19, 2024

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