Class I ยท High risk
Nexterone (amiodarone HCl)
Presence of Particulate Matter:Particulate identified as polyethylene, the primary constituent of the film and ports used to manufacture the bag in which product is packaged
National Drug Code
Is NDC 43066-0150-10 recalled?
Nexterone · 100 mL in 1 BAG (43066-150-10)
Yes — this exact package was recalled
1 FDA recall names the code 43066-0150-10 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
- amiodarone hydrochloride
- Strength
- AMIODARONE HYDROCHLORIDE 1.5 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 43066-0150
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
- 43066-0016 Cardene IV 1
- 43066-0360 Nexterone 1
- 43066-0995 Clindamycin phosphate 1
Free recall alerts
Know the day your medication is recalled
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