Class II · Moderate risk
BENAZEPRIL HCL Tablet
Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 5 mg may be potentially mislabeled as ZINC SULFATE, Capsule, 220 mg, NDC 60258013101, Pedigree: AD52993_34, EXP: 5/20/2014.
National Drug Code
Is NDC 65162-0751-10 recalled?
Benazepril Hydrochloride · 100 TABLET in 1 BOTTLE (65162-751-10)
Yes — this exact package was recalled
1 FDA recall names the code 65162-0751-10 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
- Benazepril Hydrochloride
- Strength
- BENAZEPRIL HYDROCHLORIDE 5 mg/1
- Form
- Tablet · Oral
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 65162-0751
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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