Class II · Moderate risk
Morphine Sulfate Oral Solution
Defective container: Oral solution leaking from container.
National Drug Code
Is NDC 27808-0082-01 recalled?
Morphine Sulfate · 1 BOTTLE, UNIT-DOSE in 1 CARTON (27808-082-01) / 30 mL in 1 BOTTLE, UNIT-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 27808-0082-01 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 Sulfate
- Strength
- MORPHINE SULFATE 20 mg/mL
- Form
- Solution · Oral
- Labeler
- Cranbury Pharmaceuticals, LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 27808-0082
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
- 27808-0086 Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.