Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0074-3012-07 recalled?

Duopa · 7 CARTRIDGE in 1 CARTON (0074-3012-07) / 100 mL in 1 CARTRIDGE

Yes — this exact package was recalled

1 FDA recall names the code 0074-3012-07 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
Carbidopa and Levodopa
Strength
LEVODOPA 20 mg/mL; CARBIDOPA HYDRATE 4.63 mg/mL
Form
Suspension · Enteral
Labeler
AbbVie Inc.
Type
Human Prescription Drug
Product code
0074-3012

Recalls naming this package

Class II ยท Moderate risk

Duopa (carbidopa and levodopa enteral suspension)

Failed Stability Specifications: confirmed out of specification results obtained during refrigerated material stability testing indicating that drug may settle within drug cassettes nearing the end of their refrigerated shelf-life

Terminated Stability / shelf life AbbVie Inc. NDC 0074-3012-07 D-0495-2017

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