Class II · Moderate risk
Phenazopyridine HCl
Product Mix Up. A bottle labeled as Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
National Drug Code
Is NDC 75826-0114-10 recalled?
Phenazopyridine Hydrochloride · 100 TABLET in 1 BOTTLE, PLASTIC (75826-114-10)
Yes — this exact package was recalled
2 FDA recalls name the code 75826-0114-10 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
- Phenazopyridine Hydrochloride
- Strength
- PHENAZOPYRIDINE HYDROCHLORIDE 100 mg/1
- Form
- Tablet · Oral
- Labeler
- Winder Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 75826-0114
Recalls naming this package
Class II · Moderate risk
Phenazopyridine HCl Tablets USP
Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
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
- 75826-0131 Morphine Sulfate 1
Free recall alerts
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