Class II · Moderate risk
Nystatin Oral Suspension
Subpotent drug: Out of specification for assay at the 15-month test interval.
National Drug Code
Is NDC 0121-0810-16 recalled?
Nystatin · 473 mL in 1 BOTTLE (0121-0810-16)
Yes — this exact package was recalled
3 FDA recalls name the code 0121-0810-16 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
- Nystatin
- Strength
- NYSTATIN 100000 [USP'U]/mL
- Form
- Suspension · Oral
- Labeler
- Pharmaceutical Associates, Inc.
- Type
- Human Prescription Drug
- Product code
- 0121-0810
Recalls naming this package
Class II · Moderate risk
Nystatin Oral Suspension
SubPotent Drug: Low out-of-specification results for assay testing.
Class II · Moderate risk
Nystatin Oral Suspension
Subpotent: Out of specification for assay at the 12-month time point.
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
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