Class II ยท Moderate risk
Clobazam Oral Suspension
Microbial Contamination of Non-Sterile Products: Out-of-specification results for Microbial Enumeration Tests USP <61> was observed.
National Drug Code
Is NDC 69452-0116-45 recalled?
Clobazam · 1 BOTTLE in 1 CARTON (69452-116-45) / 120 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 69452-0116-45 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
- Clobazam
- Strength
- CLOBAZAM 2.5 mg/mL
- Form
- Suspension · Oral
- Labeler
- Bionpharma Inc.
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 69452-0116
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
- 69452-0206 Doxylamine succinate and Pyridoxine hydrochloride 1
- 69452-0252 Atovaquone 1
- 69452-0435 divalproex sodium 1
Free recall alerts
Know the day your medication is recalled
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