NDC 67296-1392
Oxycodone and Acetaminophen 5 mg / 325 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-044.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Mar 18, 2020 · Class II · Aurobindo Pharma USA Inc.
CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed
Lots: Lot #: 046180056A, Exp. Date 05/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acetaminophen and Oxycodone: every company that makes it
- Form
- tablet
- Strength
- 5 mg / 325 mg
- Approval
- ANDA ANDA201972
- On the market since
- Dec 1, 2016
- Package NDCs
67296-1392-067296-1392-167296-1392-267296-1392-367296-1392-467296-1392-567296-1392-667296-1392-767296-1392-867296-1392-9- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2024
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