NDC 65862-763

Pregabalin 200 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
200 mg
Approval
ANDA ANDA205321
On the market since
Mar 29, 2023
Package NDCs
65862-763-05 65862-763-10 65862-763-78 65862-763-90
Official label
DailyMed (National Library of Medicine), updated Apr 15, 2026

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