Class III ยท Low risk
Opium Tincture
Subpotent Drug
National Drug Code
Is NDC 42799-0217-01 recalled?
Opium Tincture Deodorized · 118 mL in 1 BOTTLE, PLASTIC (42799-217-01)
Yes — this exact package was recalled
1 FDA recall names the code 42799-0217-01 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
- Morphine
- Strength
- MORPHINE 10 mg/mL
- Form
- Tincture · Oral
- Labeler
- Edenbridge Pharmaceuticals, LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 42799-0217
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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