NDC 67296-1414

Hydromorphone Hydrochloride 2 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. 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
Dec 23, 2004
Package NDCs
67296-1414-1
Official label
DailyMed (National Library of Medicine), updated Aug 25, 2026

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