NDC 40032-999

cevimeline hydrochloride 30 mg capsule

On the label: Novel Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Cevimeline: every company that makes it
Form
capsule, oral
Strength
30 mg
Approval
ANDA ANDA204746
On the market since
Dec 30, 2016
Package NDCs
40032-999-01 40032-999-03 40032-999-05
Official label
DailyMed (National Library of Medicine), updated Feb 9, 2016

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