Class III · Low risk
Benazepril HCl Tablets
Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle
National Drug Code
Is NDC 65162-0754-10 recalled?
Benazepril Hydrochloride · 100 TABLET in 1 BOTTLE (65162-754-10)
Yes — this exact package was recalled
2 FDA recalls name the code 65162-0754-10 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 40 mg/1
- Form
- Tablet · Oral
- Labeler
- Amneal Pharmaceuticals LLC
- Type
- Human Prescription Drug
- Product code
- 65162-0754
Recalls naming this package
Class II · Moderate risk
BENAZEPRIL HCL Tablet
Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 40 mg may be potentially mislabeled as NEFAZODONE HCL, Tablet, 200 mg, NDC 00093102506, Pedigree: AD46414_44, EXP: 5/16/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003931, EXP: 6/28/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD42592_1, EXP: 5/14/2014; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/25
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
- 65162-0755 Divalproex Sodium 2
- 65162-0179 Metformin Hydrochloride 1
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