NDC 0722-7076

Nabumetone 500 mg 500 mg tablet, film coated

On the label: Nexgen Pharma, Inc..

Where it's made

FactoryWhereRoleLast FDA inspection
Nexgen Pharma, Inc.Location not on fileMakes it, tests it, packages it and labels it Not inspected on record

Product details

Generic drug
Nabumetone: every company that makes it
Form
tablet, film coated
Strength
500 mg
Approval
ANDA ANDA203166
On the market since
Sep 4, 2019
Package NDCs
0722-7076-01 0722-7076-05
Official label
DailyMed (National Library of Medicine), updated Sep 27, 2019

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