NDC 72865-170

hydromorphone hydrochloride 16 mg tablet, extended release

On the label: XLCare Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Hydromorphone: every company that makes it
Form
tablet, extended release, oral
Strength
16 mg
Approval
ANDA ANDA212133
On the market since
Sep 24, 2020
Package NDCs
72865-170-01
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2024

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