Class II · Moderate risk
Metoprolol Succinate Extended-Release Tablets
Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
National Drug Code
Is NDC 70010-0780-01 recalled?
Metoprolol Succinate · 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-01)
Yes — this exact package was recalled
1 FDA recall names the code 70010-0780-01 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 25 mg/1
- Form
- Tablet, Film Coated, Extended Release · Oral
- Labeler
- Granules Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 70010-0780
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
- 70010-0001 Colchicine 1
- 70010-0029 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
- 70010-0030 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
- 70010-0031 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
- 70010-0032 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
- 70010-0034 dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate 1
Free recall alerts
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