Class II · Moderate risk
Metformin Hydrochloride Extended-Release Tablets
Presence of Foreign Tablets/Capsules: A Paracetamol 500 mg tablet was found in a 1000-count bottle of Metformin HCL ER Tablets USP, 500 mg.
National Drug Code
Is NDC 82009-0117-10 recalled?
Metformin ER 500 mg · 1000 TABLET in 1 BOTTLE (82009-117-10)
Yes — this exact package was recalled
1 FDA recall names the code 82009-0117-10 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
- Metformin ER 500 mg
- Strength
- METFORMIN HYDROCHLORIDE 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Quallent Pharmaceuticals Health LLC
- Type
- Human Prescription Drug
- Product code
- 82009-0117
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
- 82009-0032 Duloxetine 2
- 82009-0022 Omeprazole 1
- 82009-0030 Duloxetine 1
Free recall alerts
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