Class II ยท Moderate risk
Haloperidol Lactate Injection
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
National Drug Code
Is NDC 67457-0426-12 recalled?
Haloperidol Lactate · 25 VIAL in 1 CARTON (67457-426-12) / 1 mL in 1 VIAL (67457-426-00)
Yes — this exact package was recalled
1 FDA recall names the code 67457-0426-12 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
- Haloperidol Lactate
- Strength
- HALOPERIDOL LACTATE 5 mg/mL
- Form
- Injection, Solution · Intramuscular
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0426
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
- 67457-0153 Amiodarone Hydrochloride 2
- 67457-0386 Mycophenolate Mofetil 2
- 67457-0445 Rifampin 2
- 67457-0187 Aloprim 1
- 67457-0196 Thiamine Hydrochloride 1
- 67457-0197 Tranexamic Acid 1
Free recall alerts
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