Class II · Moderate risk
Metformin Hydrochloride Tablets
Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP
National Drug Code
Is NDC 67877-0217-10 recalled?
Metformin Hydrochloride · 1000 TABLET, FILM COATED in 1 BOTTLE (67877-217-10)
Yes — this exact package was recalled
1 FDA recall names the code 67877-0217-10 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 Hydrochloride
- Strength
- METFORMIN HYDROCHLORIDE 500 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Ascend Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 67877-0217
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
- 67877-0545 Cephalexin 4
- 67877-0544 Cephalexin 3
- 67877-0590 Metoprolol Succinate 3
- 67877-0446 Olmesartan Medoxomil 2
- 67877-0474 Dabigatran Etexilate 2
- 67877-0475 Dabigatran Etexilate 2
Free recall alerts
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