Class II · Moderate risk
Losartan Potassium Tablets USP
CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) detected in the active pharmaceutical ingredient
National Drug Code
Is NDC 31722-0700-05 recalled?
Losartan Potassium · 500 TABLET, FILM COATED in 1 BOTTLE (31722-700-05)
Yes — this exact package was recalled
1 FDA recall names the code 31722-0700-05 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
- Losartan Potassium
- Strength
- LOSARTAN POTASSIUM 25 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0700
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
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
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