NDC 65862-764

Pregabalin 225 mg capsule

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
Pregabalin: every company that makes it
Form
capsule, oral
Strength
225 mg
Approval
ANDA ANDA205321
On the market since
Mar 29, 2023
Package NDCs
65862-764-05 65862-764-10 65862-764-78 65862-764-90
Official label
DailyMed (National Library of Medicine), updated Apr 15, 2026

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