Class II · Moderate risk
Penicillin V Potassium for Oral Solution
Subpotent
National Drug Code
Is NDC 0093-4125-73 recalled?
Penicillin V Potassium · 100 mL in 1 BOTTLE (0093-4125-73)
Yes — this exact package was recalled
3 FDA recalls name the code 0093-4125-73 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
- Penicillin V Potassium
- Strength
- PENICILLIN V POTASSIUM 125 mg/5mL
- Form
- Powder, for Solution · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-4125
Recalls naming this package
Class II · Moderate risk
PENICILLIN V POT for Oral Solution
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Class III · Low risk
Penicillin V Potassium for Oral Solution
Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
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
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