Class II ยท Moderate risk
Carvedilol 25 mg
A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged into 180 count bottles.
National Drug Code
Is NDC 70518-1826-01 recalled?
Carvedilol · 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1826-1)
Yes — this exact package was recalled
1 FDA recall names the code 70518-1826-01 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
- Carvedilol
- Strength
- CARVEDILOL 25 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Remedyrepack INC.
- Type
- Human Prescription Drug
- Product code
- 70518-1826
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
- 70518-1220 See recall 2
- 70518-1560 Doxazosin 2
- 70518-3519 See recall 2
- 70518-3772 Clindamycin Hydrochloride 2
- 70518-0060 See recall 1
- 70518-0064 See recall 1
Free recall alerts
Know the day your medication is recalled
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