Class II ยท Moderate risk
Eszopiclone Tablets
Shortfill: customer complaints of one to three tablets were reported missing from 30 count bottles.
National Drug Code
Is NDC 33342-0299-07 recalled?
Eszopiclone · 30 TABLET, FILM COATED in 1 BOTTLE (33342-299-07)
Yes — this exact package was recalled
1 FDA recall names the code 33342-0299-07 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
- Eszopiclone
- Strength
- ESZOPICLONE 1 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Macleods Pharmaceuticals Limited
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 33342-0299
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
- 33342-0050 Losartan potassium and Hydrochlorothiazide 4
- 33342-0052 Losartan potassium and Hydrochlorothiazide 4
- 33342-0045 Losartan potassium 3
- 33342-0031 Pramipexole dihydrochloride 2
- 33342-0051 Losartan potassium and Hydrochlorothiazide 2
- 33342-0192 AMLODIPINE and OLMESARTAN medoxomil 2
Free recall alerts
Know the day your medication is recalled
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