Class III · Low risk
Fexofenadine HCl
Failed dissolution specifications
National Drug Code
Is NDC 43598-0823-31 recalled?
Fexofenadine HCl and Pseudoephedrine HCI · 6 BLISTER PACK in 1 CARTON (43598-823-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 43598-0823-31 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
- Fexofenadine HCl and Pseudoephedrine HCI
- Strength
- FEXOFENADINE HYDROCHLORIDE 60 mg/1; PSEUDOEPHEDRINE…
- Form
- Tablet, Extended Release
- Labeler
- Dr. Reddy's Laboratories Inc.
- Type
- Drug for Further Processing
- Product code
- 43598-0823
Recalls naming this package
Class III · Low risk
Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended…
Failed dissolution specifications
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
- 43598-0315 Amlodipine besylate and Atorvastatin calcium 2
- 43598-0405 Phytonadione Phytonadione 2
- 43598-0477 See recall 2
- 43598-0510 Esomeprazole Magnesium 2
- 43598-0561 Lansoprazole 2
- 43598-0743 Ezetimibe and Simvastatin 2
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