Class III · Low risk
Pioglitazone and Metformin Hydrochloride Tablets
Subpotent Drug: Out of specification assay result, below specification, for two lots of Pioglitazone And Metformin Hydrochloride Tablets.
National Drug Code
Is NDC 33342-0176-09 recalled?
Pioglitazone and metformin hydrochloride · 60 TABLET in 1 BOTTLE (33342-176-09)
Yes — this exact package was recalled
1 FDA recall names the code 33342-0176-09 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
- Pioglitazone and metformin hydrochloride
- Strength
- METFORMIN HYDROCHLORIDE 500 mg/1; PIOGLITAZONE…
- Form
- Tablet · Oral
- Labeler
- Macleods Pharmaceuticals Limited
- Type
- Human Prescription Drug
- Product code
- 33342-0176
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
- 33342-0050 Losartan potassium and Hydrochlorothiazide 4
- 33342-0052 Losartan potassium and Hydrochlorothiazide 4
- 33342-0045 Losartan potassium 3
- 33342-0031 Pramipexole dihydrochloride 2
- 33342-0051 Losartan potassium and Hydrochlorothiazide 2
- 33342-0192 AMLODIPINE and OLMESARTAN medoxomil 2
Free recall alerts
Know the day your medication is recalled
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