NDC 60687-579

Hydromorphone Hydrochloride 2 mg tablet

On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from SpecGx LLC's NDC 0406-3243.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
SpecGx LLCHobart, NY, United StatesMakes it and tests it No problems foundMar 13, 2020 · 6 inspections

Repackaging site

Product details

Generic drug
Hydromorphone: every company that makes it
Form
tablet, oral
Strength
2 mg
Approval
ANDA ANDA076855
On the market since
May 11, 2021
Package NDCs
60687-579-01 60687-579-11
Official label
DailyMed (National Library of Medicine), updated Feb 27, 2026

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