Class II · Moderate risk
Epi-Pen 2-Pak
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 49502-0500-02 recalled?
Epipen · 2 CONTAINER in 1 CARTON (49502-500-02) / 1 SYRINGE, GLASS in 1 CONTAINER (49502-500-01) / .3 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
4 FDA recalls name the code 49502-0500-02 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.
2 of these recalls are still ongoing.
- Active ingredient
- epinephrine
- Strength
- EPINEPHRINE .3 mg/.3mL
- Form
- Injection · Intramuscular
- Labeler
- Viatris Specialty LLC
- Type
- Human Prescription Drug
- Product code
- 49502-0500
Recalls naming this package
Class II · Moderate risk
Epinephrine Injection
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Class I · High risk
EpiPen Jr. 2-Pak
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Class I · High risk
EpiPen 2-Pak
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
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
- 49502-0501 Epipen Jr 2
- 49502-0101 Epinephrine 1
- 49502-0102 Epinephrine 1
- 49502-0196 See recall 1
- 49502-0393 See recall 1
- 49502-0394 See recall 1
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