Class II ยท Moderate risk
Metoprolol Succinate Extended-Release Tablets
Failed Dissolution Specifications
National Drug Code
Is NDC 45963-0677-11 recalled?
metoprolol succinate · 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-677-11)
Yes — this exact package was recalled
1 FDA recall names the code 45963-0677-11 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 succinate
- Strength
- METOPROLOL SUCCINATE 100 mg/1
- Form
- Tablet, Film Coated, Extended Release
- Labeler
- Actavis Pharma, Inc.
- Type
- Drug for Further Processing
- Product code
- 45963-0677
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
- 45963-0676 metoprolol succinate 2
- 45963-0304 dextroamphetamine sulfate 1
- 45963-0305 dextroamphetamine sulfate 1
- 45963-0343 Desipramine Hydrochloride 1
- 45963-0412 See recall 1
- 45963-0555 Gabapentin 1
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