Class II · Moderate risk
Hydrocodone Bitartrate and Acetaminophen Tablets
Product Mix-up
National Drug Code
Is NDC 31722-0997-01 recalled?
Hydrocodone Bitartrate and Acetaminophen · 100 TABLET in 1 BOTTLE (31722-997-01)
Yes — this exact package was recalled
1 FDA recall names the code 31722-0997-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Hydrocodone Bitartrate and Acetaminophen
- Strength
- HYDROCODONE BITARTRATE 10 mg/1; ACETAMINOPHEN 325 mg/1
- Form
- Tablet · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 31722-0997
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
Free recall alerts
Know the day your medication is recalled
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