NDC 53002-0102
Acetaminophen And Codeine Phosphate 30 mg / 300 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from SpecGx LLC's NDC 0406-0484.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| SpecGx LLC | Hobart, NY, United States | Makes it and tests it | No problems foundMar 13, 2020 · 6 inspections |
| SpecGx LLC | St. Louis, MO, United States | Makes the active ingredient | Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections |
| SpecGx LLC | Greenville, IL, United States | Makes the active ingredient | Problems found, fixed voluntarilyFeb 27, 2026 · 5 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Acetaminophen and Codeine: every company that makes it
- Form
- tablet
- Strength
- 30 mg / 300 mg
- Approval
- ANDA ANDA040419
- On the market since
- May 31, 2001
- Package NDCs
53002-0102-153002-0102-253002-0102-353002-0102-5- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2023
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