NDC 71335-0723

Hydromorphone Hydrochloride 4 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurolife Pharma LLC's NDC 13107-108.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Hydromorphone: every company that makes it
Form
tablet, oral
Strength
4 mg
Approval
ANDA ANDA205814
On the market since
May 17, 2016
Package NDCs
71335-0723-0 71335-0723-1 71335-0723-2 71335-0723-3 71335-0723-4 71335-0723-5 71335-0723-6 71335-0723-7 71335-0723-8 71335-0723-9
Official label
DailyMed (National Library of Medicine), updated Aug 9, 2024

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