Class II · Moderate risk
Metoprolol Tartrate Tablets USP
Presence of Foreign Substance: metal in tablet
National Drug Code
Is NDC 52817-0360-00 recalled?
Metoprolol Tartrate · 1000 TABLET, FILM COATED in 1 BOTTLE (52817-360-00)
Yes — this exact package was recalled
2 FDA recalls name the code 52817-0360-00 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.
1 of these recalls is still ongoing.
- Active ingredient
- Metoprolol Tartrate
- Strength
- METOPROLOL TARTRATE 25 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- TruPharma LLC
- Type
- Human Prescription Drug
- Product code
- 52817-0360
Recalls naming this package
Class II · Moderate risk
Metoprolol Tartrate Tablets
Complaint received of foreign matter (metal) embedded in tablet.
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
- 52817-0196 Tramadol Hydrochloride 1
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