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 70518-0218-00 recalled?
Phenazopyridine Hydrochloride · 6 TABLET in 1 BOTTLE, PLASTIC (70518-0218-0)
Yes — this exact package was recalled
1 FDA recall names the code 70518-0218-00 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
- Remedyrepack INC.
- Type
- Human Prescription Drug
- Product code
- 70518-0218
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
- 70518-1220 See recall 2
- 70518-1560 Doxazosin 2
- 70518-3519 See recall 2
- 70518-3772 Clindamycin Hydrochloride 2
- 70518-0060 See recall 1
- 70518-0064 See recall 1
Free recall alerts
Know the day your medication is recalled
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