Class II · Moderate risk
Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg
Subpotent drug: Out of specification for assay of naloxone and buprenorphine (low)
National Drug Code
Is NDC 47781-0355-03 recalled?
Buprenorphine and Naloxone Sublingual Film · 30 POUCH in 1 CARTON (47781-355-03) / 1 FILM in 1 POUCH (47781-355-11)
Yes — this exact package was recalled
1 FDA recall names the code 47781-0355-03 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
- Buprenorphine and Naloxone
- Strength
- BUPRENORPHINE HYDROCHLORIDE 2 mg/1; NALOXONE HYDROCHLORIDE…
- Form
- Film · Buccal, Sublingual
- Labeler
- Alvogen Inc.
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 47781-0355
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
- 47781-0356 Buprenorphine and Naloxone Sublingual Film 1
- 47781-0368 See recall 1
Free recall alerts
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