NDC 27241-125

Ranolazine 500 mg tablet, extended release

On the label: Ajanta Pharma USA Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ajanta Pharma LimitedBharuch, IndiaMakes it No problems foundJun 23, 2023 · 3 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
Ranolazine: every company that makes it
Form
tablet, extended release, oral
Strength
500 mg
Approval
ANDA ANDA210054
On the market since
Aug 23, 2019
Package NDCs
27241-125-02 27241-125-05
Official label
DailyMed (National Library of Medicine), updated Oct 28, 2025

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