Class I ยท High risk
Clonazepam Orally Disintegrating Tablets
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
National Drug Code
Is NDC 49884-0307-52 recalled?
Clonazepam
Yes — this exact package was recalled
1 FDA recall names the code 49884-0307-52 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
- clonazepam
- Strength
- CLONAZEPAM .25 mg/1
- Form
- Tablet, Orally Disintegrating · Oral
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 49884-0307
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
- 49884-0125 See recall 2
- 49884-0306 Clonazepam 2
- 49884-0922 See recall 2
- 49884-0034 See recall 1
- 49884-0035 See recall 1
- 49884-0038 See recall 1
Free recall alerts
Know the day your medication is recalled
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