Class II ยท Moderate risk
Celecoxib Capsules
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
National Drug Code
Is NDC 62332-0142-71 recalled?
Celecoxib · 500 CAPSULE in 1 BOTTLE (62332-142-71)
Yes — this exact package was recalled
1 FDA recall names the code 62332-0142-71 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
- Celecoxib
- Strength
- CELECOXIB 200 mg/1
- Form
- Capsule · Oral
- Labeler
- Alembic Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 62332-0142
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
- 62332-0508 Bromfenac Ophthalmic Solution 0.09% 2
- 62332-0087 Telmisartan 1
- 62332-0097 Aripiprazole 1
- 62332-0115 Metoprolol Tartrate and Hydrochlorothiazide 1
- 62332-0175 Fesoterodine Fumarate 1
- 62332-0176 Fesoterodine Fumarate 1
Free recall alerts
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