Class III ยท Low risk
Morphine Sulfate Oral Solution 100 mg / 5 mL
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
National Drug Code
Is NDC 75826-0131-01 recalled?
Morphine Sulfate · 30 mL in 1 BOTTLE, PLASTIC (75826-131-01)
Yes — this exact package was recalled
1 FDA recall names the code 75826-0131-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Morphine Sulfate
- Strength
- MORPHINE SULFATE 100 mg/5mL
- Form
- Solution · Oral
- Labeler
- Winder Laboratories LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 75826-0131
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
- 75826-0114 Phenazopyridine Hydrochloride 2
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.