Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0378-8020-77 recalled?

Fluvastatin Sodium · 90 CAPSULE in 1 BOTTLE, PLASTIC (0378-8020-77)

Yes — this exact package was recalled

1 FDA recall names the code 0378-8020-77 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
fluvastatin
Strength
FLUVASTATIN SODIUM 20 mg/1
Form
Capsule · Oral
Labeler
Mylan Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
0378-8020

Recalls naming this package

Class II ยท Moderate risk

Fluvastatin

Labeling: Label Mixup: FLUVASTATIN, Capsule, 20 mg may have potentially been mislabeled as the following drug: ACETAMINOPHEN/ BUTALBITAL/ CAFFEINE, Tablet, 325 mg/50 mg/40 mg, NDC 00603254421, Pedigree: W002654, EXP: 6/4/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-910-2014

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