NDC 65862-670

Repaglinide 0.5 mg tablet

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Product details

Generic drug
Repaglinide: every company that makes it
Form
tablet, oral
Strength
0.5 mg
Approval
ANDA ANDA203820
On the market since
Jan 22, 2014
Package NDCs
65862-670-01 65862-670-05 65862-670-99
Official label
DailyMed (National Library of Medicine), updated May 14, 2024

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