NDC 0722-7183

Mecamylamine Hydrochloride 2.5 mg tablet

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
Mecamylamine: every company that makes it
Form
tablet
Strength
2.5 mg
Approval
ANDA ANDA204054
On the market since
Mar 19, 2013
Package NDCs
0722-7183-01
Official label
DailyMed (National Library of Medicine), updated Sep 4, 2019

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