FDA Drug Recalls

Recalls / Firms / Aurolife Pharma, LLC

Aurolife Pharma, LLC

14 FDA drug recalls on record.

DateClassDrugStatus
2023-05-18Class IIIGlycopyrrolateTerminated
2022-12-16Class IIGlycopyrrolateOngoing
2022-03-17Class IIGlycopyrrolateTerminated
2019-08-23Class IIAllergy Relief (fexofenadine hydrochrloride) tablets, 180 mg, 5-count carton, Good NeighboTerminated
2019-08-23Class IIAllergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count Terminated
2019-08-23Class IIFexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 62011Terminated
2019-08-23Class IIAllergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count cartons, DISCOUNT drug Terminated
2019-08-23Class IIAllergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed byTerminated
2019-08-23Class IIfexofenadine hydrochloride tablets USP, 180 mg, 150-count bottle, Member's Mark, DistributTerminated
2019-08-23Class IIFexofenadine HCL Tablets USP, 180 mg, 500's BRITE STOCK; Manufactured for: Aurohealth LLC.Terminated
2019-08-23Class IIFexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 30-count carton (NDC 70677-Terminated
2019-08-23Class IIFexofenadine Hydrochrloride Tablets USP, 180 mg, 100-count bottle, Distributed by: AuroheaTerminated
2019-08-23Class IIAllergy Relief (Fexofenadine HCl) tablets USP, 180 mg, 15-count cartons, equate, DistributTerminated
2019-08-23Class IIWal-Fex (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 5-count cartons, Distributed By:Terminated