Class II · Moderate risk
Losartan Potassium Tablets
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
National Drug Code
Is NDC 64380-0933-08 recalled?
LOSARTAN POTASSIUM 25 mg · 1000 TABLET, FILM COATED in 1 BOTTLE (64380-933-08)
Yes — this exact package was recalled
2 FDA recalls name the code 64380-0933-08 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
- Losartan Potassium
- Strength
- LOSARTAN POTASSIUM 25 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Strides Pharma Science Limited
- Type
- Human Prescription Drug
- Product code
- 64380-0933
Recalls naming this package
Class II · Moderate risk
Losartan Potassium Tablets
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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
- 64380-0861 Potassium Chloride 2
- 64380-0151 Testosterone 1
- 64380-0152 Testosterone 1
- 64380-0474 Atomoxetine 1
- 64380-0713 Benzonatate 1
- 64380-0721 Tacrolimus 1
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