NDC 0406-0484

Acetaminophen And Codeine Phosphate 30 mg / 300 mg tablet

On the label: SpecGx LLC.

United States: 3

Where it's 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

Product details

Generic drug
Acetaminophen and Codeine: every company that makes it
Form
tablet, oral
Strength
30 mg / 300 mg
Approval
ANDA ANDA040419
On the market since
May 31, 2001
Package NDCs
0406-0484-01 0406-0484-03 0406-0484-10 0406-0484-20 0406-0484-23 0406-0484-50 0406-0484-62
Official label
DailyMed (National Library of Medicine), updated Jun 12, 2026

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