Class II ยท Moderate risk
Duloxetine Delayed-Release Capsules
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
National Drug Code
Is NDC 51991-0750-33 recalled?
Duloxetine Delayed-Release · 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33)
Yes — this exact package was recalled
1 FDA recall names the code 51991-0750-33 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
- Duloxetine Hydrochloride
- Strength
- DULOXETINE HYDROCHLORIDE 40 mg/1
- Form
- Capsule, Delayed Release Pellets · Oral
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Type
- Human Prescription Drug
- Product code
- 51991-0750
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
- 51991-0748 Duloxetine Delayed-Release 11
- 51991-0747 Duloxetine Delayed-Release 6
- 51991-0746 Duloxetine Delayed-Release 3
- 51991-0014 See recall 1
- 51991-0064 See recall 1
- 51991-0457 See recall 1
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