NDC 60760-871

Hydrocodone Bitartrate And Acetaminophen 10 mg / 325 mg tablet

On the label: St. Mary's Medical Park Pharmacy. It's repackaged: St. Mary's Medical Park Pharmacy rebottles it from SpecGx LLC's NDC 0406-0125.

United States: 3

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
SpecGx LLCSt. Louis, MO, United StatesMakes the active ingredient Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections
SpecGx LLCGreenville, IL, United StatesMakes the active ingredient Problems found, fixed voluntarilyFeb 27, 2026 · 5 inspections

Repackaging site

Product details

Generic drug
Acetaminophen and Hydrocodone: every company that makes it
Form
tablet, oral
Strength
10 mg / 325 mg
Approval
ANDA ANDA040400
On the market since
Jul 26, 2000
Package NDCs
60760-871-30 60760-871-60
Official label
DailyMed (National Library of Medicine), updated May 20, 2026

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