Class II · 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 68382-0095-05 recalled?
Carvedilol · 500 TABLET, FILM COATED in 1 BOTTLE (68382-095-05)
Yes — this exact package was recalled
2 FDA recalls name the code 68382-0095-05 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
- Zydus Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 68382-0095
Recalls naming this package
Class II · Moderate risk
Carvedilol Tablets
Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were found in the bottle
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
- 68382-0021 Venlafaxine 2
- 68382-0033 See recall 2
- 68382-0099 Paroxetine 2
- 68382-0110 Bromocriptine mesylate 2
- 68382-0123 Amlodipine Besylate 2
- 68382-0196 See recall 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.