Class II ยท Moderate risk
Jentadueto XR
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 0597-0275-33 recalled?
Jentadueto XR · 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0597-0275-33)
Yes — this exact package was recalled
1 FDA recall names the code 0597-0275-33 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
- linagliptin and metformin hydrochloride
- Strength
- LINAGLIPTIN 5 mg/1; METFORMIN HYDROCHLORIDE 1000 mg/1
- Form
- Tablet, Film Coated, Extended Release · Oral
- Labeler
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 0597-0275
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
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