Class III · Low risk
Pramipexole Dihydrochloride Tablets 0.125 mg
Subpotent Drug: Out of specification result during stability study in Pramipexole Dihydrochloride Tablets 0.125 mg
National Drug Code
Is NDC 33342-0031-10 recalled?
Pramipexole dihydrochloride · 90 TABLET in 1 BOTTLE (33342-031-10)
Yes — this exact package was recalled
2 FDA recalls name the code 33342-0031-10 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
- Pramipexole dihydrochloride
- Strength
- PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1
- Form
- Tablet · Oral
- Labeler
- Macleods Pharmaceuticals Limited
- Type
- Human Prescription Drug
- Product code
- 33342-0031
Recalls naming this package
Class II · Moderate risk
Pramipexole Dihydrochloride Tablets 0.125 mg
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
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
- 33342-0051 Losartan potassium and Hydrochlorothiazide 2
- 33342-0192 AMLODIPINE and OLMESARTAN medoxomil 2
- 33342-0022 See recall 1
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