Class II · Moderate risk
Metoprolol Tartrate Tablets USP 100 mg
Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.
National Drug Code
Is NDC 65862-0064-99 recalled?
Metoprolol Tartrate · 1000 TABLET, FILM COATED in 1 BOTTLE (65862-064-99)
Yes — this exact package was recalled
1 FDA recall names the code 65862-0064-99 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
- Metoprolol Tartrate
- Strength
- METOPROLOL TARTRATE 100 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Aurobindo Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 65862-0064
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
- 65862-0053 Simvastatin 2
- 65862-0420 Sulfamethoxazole and Trimethoprim 2
- 65862-0573 Valsartan 2
- 65862-0739 Amlodipine and valsartan 2
- 65862-0840 Moxifloxacin 2
- 65862-0010 Metformin Hydrochloride 1
Free recall alerts
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