Class II · Moderate risk
Acetaminophen Oral Suspension
cGMP Deviations: Product manufactured with contaminated raw ingredient.
National Drug Code
Is NDC 68094-0330-59 recalled?
Acetaminophen
Yes — this exact package was recalled
1 FDA recall names the code 68094-0330-59 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
- Acetaminophen
- Strength
- ACETAMINOPHEN 160 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Precision Dose, Inc.
- Type
- Human OTC Drug
- Product code
- 68094-0330
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
- 68094-0301 See recall 2
- 68094-0028 See recall 1
- 68094-0073 Glycopyrrolate 1
- 68094-0081 Lidocaine Hydrochloride 1
- 68094-0204 See recall 1
- 68094-0231 Acetaminophen 1
Free recall alerts
Know the day your medication is recalled
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