Class II ยท Moderate risk
Celecoxib Capsules
Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
National Drug Code
Is NDC 50268-0169-15 recalled?
Celecoxib · 50 BLISTER PACK in 1 BOX (50268-169-15) / 1 CAPSULE in 1 BLISTER PACK (50268-169-11)
Yes — this exact package was recalled
1 FDA recall names the code 50268-0169-15 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
- AvPAK
- Type
- Human Prescription Drug
- Product code
- 50268-0169
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
- 50268-0068 carboxymethylcellulose sodium 4
- 50268-0069 Amantadine HCl 3
- 50268-0517 See recall 2
- 50268-0678 Polyvinyl Alcohol 2
- 50268-0043 Artificial Tears 1
- 50268-0061 Acyclovir 1
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