Class II · Moderate risk
Fentanyl Citrate USP
CGMP Deviations: Received notice from supplier that there is potential glass contamination.
National Drug Code
Is NDC 49452-0032-06 recalled?
Fentanyl Citrate · .05 g in 1 BOTTLE, GLASS (49452-0032-6)
Yes — this exact package was recalled
1 FDA recall names the code 49452-0032-06 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
- Fentanyl Citrate
- Strength
- FENTANYL CITRATE 1 g/g
- Form
- Crystal
- Labeler
- Spectrum Chemical and Laboratory Products
- Type
- Bulk Ingredient · DEA CII
- Product code
- 49452-0032
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.
Free recall alerts
Know the day your medication is recalled
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