Class II ยท Moderate risk
DESIPRAMINE HCL Tablet
Labeling: Label Mixup; DESIPRAMINE HCL Tablet, 50 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD30140_4, EXP: 5/7/2014.
National Drug Code
Is NDC 45963-0343-02 recalled?
Desipramine Hydrochloride · 100 TABLET, FILM COATED in 1 BOTTLE (45963-343-02)
Yes — this exact package was recalled
1 FDA recall names the code 45963-0343-02 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
- Desipramine Hydrochloride
- Strength
- DESIPRAMINE HYDROCHLORIDE 50 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 45963-0343
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
- 45963-0676 metoprolol succinate 2
- 45963-0304 dextroamphetamine sulfate 1
- 45963-0305 dextroamphetamine sulfate 1
- 45963-0412 See recall 1
- 45963-0555 Gabapentin 1
- 45963-0556 Gabapentin 1
Free recall alerts
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