Class II ยท Moderate risk
Adrenalin (epinephrine)
Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
National Drug Code
Is NDC 42023-0159-25 recalled?
Adrenalin · 25 VIAL in 1 CARTON (42023-159-25) / 1 mL in 1 VIAL (42023-159-01)
Yes — this exact package was recalled
1 FDA recall names the code 42023-0159-25 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
- epinephrine
- Strength
- EPINEPHRINE 1 mg/mL
- Form
- Injection · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug
- Product code
- 42023-0159
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
- 42023-0179 Buprenorphine Hydrochloride 4
- 42023-0103 See recall 1
- 42023-0116 Pitocin 1
- 42023-0168 Adrenalin 1
- 42023-0206 See recall 1
- 42023-0237 Vasostrict 1
Free recall alerts
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