Class II · Moderate risk
Ropinirole
cGMP deviations
National Drug Code
Is NDC 72189-0364-30 recalled?
Ropinirole · 30 TABLET, FILM COATED in 1 BOTTLE (72189-364-30)
Yes — this exact package was recalled
2 FDA recalls name the code 72189-0364-30 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
- Ropinirole
- Strength
- ROPINIROLE HYDROCHLORIDE .25 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Direct_Rx
- Type
- Human Prescription Drug
- Product code
- 72189-0364
Recalls naming this package
Class II · Moderate risk
Ropinirole
cGMP deviations
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
- 72189-0058 See recall 1
- 72189-0064 Metformin Hydrochloride Extended Release 1
- 72189-0076 See recall 1
- 72189-0121 See recall 1
- 72189-0167 Losartan Potassium and Hydrochlorothiazide 1
- 72189-0213 See recall 1
Free recall alerts
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