Class I · High risk
FENTANYL Transdermal System
Product Mix-Up: Customer complaint that their carton labeled as Fentanyl Transdermal Systems, 12 mcg/h contained five patches labeled and containing 50 mcg/h.
National Drug Code
Is NDC 47781-0423-47 recalled?
Fentanyl system · 5 POUCH in 1 CARTON (47781-423-47) / 1 PATCH in 1 POUCH (47781-423-11)
Yes — this exact package was recalled
1 FDA recall names the code 47781-0423-47 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
- Strength
- FENTANYL 12.5 ug/1
- Form
- Patch · Transdermal
- Labeler
- Alvogen
- Type
- Human Prescription Drug · DEA CII
- Product code
- 47781-0423
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
- 47781-0303 Nitrofurantoin Monohydrate/ Macrocrystalline 3
- 47781-0304 See recall 1
- 47781-0306 See recall 1
- 47781-0307 See recall 1
- 47781-0355 Buprenorphine and Naloxone Sublingual Film 1
- 47781-0356 Buprenorphine and Naloxone Sublingual Film 1
Free recall alerts
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