NDC 43598-297

pregabalin 225 mg capsule

On the label: Dr. Reddy's Laboratories Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Dr. Reddy's Laboratories LimitedSrikakulam, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Pregabalin: every company that makes it
Form
capsule, oral
Strength
225 mg
Approval
ANDA ANDA209664
On the market since
Jul 19, 2019
Package NDCs
43598-297-05 43598-297-66 43598-297-78 43598-297-79 43598-297-90
Official label
DailyMed (National Library of Medicine), updated May 20, 2025

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