NDC 13107-045 – Oxycodone and Acetaminophen
Oxycodone Hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral
Product NDC13107-045
Product details
- Brand name
- Oxycodone and Acetaminophen
- Generic name
- Oxycodone and Acetaminophen
- Labeler
- Aurolife Pharma, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA201972
- Marketed since
- July 15, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 7.5 mg/1
- Acetaminophen 325 mg/1
Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 13107-045-01 | 100 TABLET in 1 BOTTLE (13107-045-01) | Jul 15, 2013 |
| 13107-045-05 | 500 TABLET in 1 BOTTLE (13107-045-05) | Jul 15, 2013 |
| 13107-045-30 | 30 TABLET in 1 BOTTLE (13107-045-30) | Jul 15, 2013 |
| 13107-045-99 | 1000 TABLET in 1 BOTTLE (13107-045-99) | Jul 15, 2013 |
Recalls mentioning this NDC
- D-1237-2020 Apr 22, 2020 · Class II
CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed
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