Class II · Moderate risk
FLECAINIDE ACETATE Tablet
Labeling:Label Mixup; FLECAINIDE ACETATE Tablet, 50 mg may be potentially mislabeled as VITAMIN B COMPLEX W/C, Tablet, NDC 00904026013, Pedigree: AD46419_7, EXP: 5/16/2014.
National Drug Code
Is NDC 65162-0641-10 recalled?
Flecainide Acetate · 100 TABLET in 1 BOTTLE (65162-641-10)
Yes — this exact package was recalled
1 FDA recall names the code 65162-0641-10 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
- Flecainide Acetate
- Strength
- FLECAINIDE ACETATE 50 mg/1
- Form
- Tablet · Oral
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 65162-0641
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
- 65162-0178 Metformin Hydrochloride 4
- 65162-0212 Extended Phenytoin Sodium 3
- 65162-0253 See recall 2
- 65162-0668 See recall 2
- 65162-0754 Benazepril Hydrochloride 2
- 65162-0755 Divalproex Sodium 2
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