Class II ยท Moderate risk
Fluoxetine Capsules
Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor.
National Drug Code
Is NDC 68645-0130-54 recalled?
Fluoxetine · 30 CAPSULE in 1 BOTTLE (68645-130-54)
Yes — this exact package was recalled
1 FDA recall names the code 68645-0130-54 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
- Fluoxetine
- Strength
- FLUOXETINE HYDROCHLORIDE 20 mg/1
- Form
- Capsule · Oral
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Type
- Human Prescription Drug
- Product code
- 68645-0130
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
- 68645-0494 See recall 2
- 68645-0445 See recall 1
- 68645-0493 See recall 1
- 68645-0523 Sertraline Hydrochloride 1
- 68645-0545 See recall 1
- 68645-0577 See recall 1
Free recall alerts
Know the day your medication is recalled
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