Class II · Moderate risk
metformin HCL ER 500 mg
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
National Drug Code
Is NDC 72789-0009-30 recalled?
Metformin Hydrochloride Extended Release · 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-009-30)
Yes — this exact package was recalled
2 FDA recalls name the code 72789-0009-30 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, Extended Release · Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 72789-0009
Recalls naming this package
Class II · Moderate risk
metFORMIN HCL ER 500 mg
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
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
- 72789-0163 LOSARTAN POTASSIUM 25 mg 1
- 72789-0164 LOSARTAN POTASSIUM 50 mg 1
- 72789-0165 LOSARTAN POTASSIUM 100 mg 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.