NDC 21695-243

Acetaminophen And Codeine Phosphate 60 mg / 300 mg tablet

On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from SpecGx LLC's NDC 0406-0484.

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

Product details

Generic drug
Acetaminophen and Codeine: every company that makes it
Form
tablet
Strength
60 mg / 300 mg
Approval
ANDA ANDA040419
On the market since
Jun 29, 2009
Package NDCs
21695-243-28 21695-243-60
Official label
DailyMed (National Library of Medicine), updated Dec 1, 2009

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