NDC 53489-141

Quinidine Gluconate 324 mg tablet, extended release

On the label: Caraco Pharmaceutical Laboratories, Ltd..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Frontida BioPharm, LLCPhiladelphia, PA, United StatesMakes it, tests it and packages it No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action

Product details

Generic drug
Quinidine: every company that makes it
Form
tablet, extended release, oral
Strength
324 mg
Approval
ANDA ANDA089338
On the market since
Feb 10, 1987
Package NDCs
53489-141-01 53489-141-03 53489-141-05 53489-141-06 53489-141-07 53489-141-10 53489-141-90
Official label
DailyMed (National Library of Medicine), updated Feb 1, 2018

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