Class II ยท Moderate risk
CITALOPRAM Tablets
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
National Drug Code
Is NDC 0378-6232-01 recalled?
Citalopram · 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01)
Yes — this exact package was recalled
1 FDA recall names the code 0378-6232-01 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
- citalopram
- Strength
- CITALOPRAM HYDROBROMIDE 20 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 0378-6232
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
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