NDC 13107-109

Hydromorphone Hydrochloride 8 mg tablet

On the label: Aurolife Pharma LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action

Product details

Generic drug
Hydromorphone: every company that makes it
Form
tablet, oral
Strength
8 mg
Approval
ANDA ANDA205814
On the market since
May 17, 2016
Package NDCs
13107-109-01 13107-109-05 13107-109-20 13107-109-99
Official label
DailyMed (National Library of Medicine), updated Dec 25, 2023

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