Class III · Low risk
Amlodipine Besylate Tablets
Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.
National Drug Code
Is NDC 68180-0721-03 recalled?
Amlodipine Besylate · 1000 TABLET in 1 BOTTLE (68180-721-03)
Yes — this exact package was recalled
1 FDA recall names the code 68180-0721-03 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
- Amlodipine Besylate
- Strength
- AMLODIPINE BESYLATE 10 mg/1
- Form
- Tablet · Oral
- Labeler
- Lupin Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 68180-0721
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
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
Free recall alerts
Know the day your medication is recalled
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