Class II ยท Moderate risk
Nexterone (amiodarone HCI)
CGMP Deviations
National Drug Code
Is NDC 43066-0360-20 recalled?
Nexterone · 200 mL in 1 BAG (43066-360-20)
Yes — this exact package was recalled
1 FDA recall names the code 43066-0360-20 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
- amiodarone hydrochloride
- Strength
- AMIODARONE HYDROCHLORIDE 1.8 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 43066-0360
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
- 43066-0150 Nexterone 1
- 43066-0995 Clindamycin phosphate 1
Free recall alerts
Know the day your medication is recalled
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