Class II ยท Moderate risk
Carvedilol Tablets USP
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
National Drug Code
Is NDC 0904-7307-61 recalled?
Carvedilol · 100 BLISTER PACK in 1 CARTON (0904-7307-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0904-7307-61 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.
1 of these recalls is still ongoing.
- Active ingredient
- Carvedilol
- Strength
- CARVEDILOL 12.5 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Major Pharmaceuticals
- Type
- Human Prescription Drug
- Product code
- 0904-7307
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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