FDA Drug Recalls

Recalls / Active ingredient / Nitrofurantoin

Nitrofurantoin

8 FDA drug recalls involving the active ingredient “Nitrofurantoin.

DateClassProductFirm
2024-07-09Class IINitrofurantoin Capsules, USP (Macrocrystals), 100 mg, Rx Only, 100 capsules per bottle, Manufactured by: SidmaSUN PHARMACEUTICAL INDUSTRIES INC
2021-03-15Class IINitrofurantoin Macrocrystals Capsules 25 mg 100 Capsules Rx Only NDC 47781-306-01 Manufactured by: Norwich PhaCardinal Health Inc.
2019-07-24Class IIMacrobid Urinary Tract Anitbacterial, 100 mg, 100-count bottle, Rx Only, Mfg. by: Norwich Pharmaceuticals, InAlvogen, Inc
2019-07-24Class IINitrofurantoin Monohydrate/Macrycrystals Capsules, 100 mg, 100-count bottle, Rx Only, Distributed by: Alvogen,Alvogen, Inc
2018-12-21Class IINitrofurantoin Oral Suspension, USP, 25mg/5mL, 230 mL bottle, Rx only, Manufactured by: Novel Laboratories, InLUPIN SOMERSET
2018-11-02Class IIINitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, packaged in a) 100-capsule bottles (NDC 0185-Sandoz Inc
2018-06-28Class IINitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, IncLUPIN SOMERSET
2015-04-21Class IINITROFURANTOIN MONOHYDRATE/MACROCRYSTALS CAPSULES, 100 mg, 100 count bottle, Rx Only --- Distributed by AlvogeAlvogen, Inc