FDA Drug Recalls

Recalls / Generics / Desipramine Hydrochloride

Desipramine Hydrochloride

6 FDA drug recalls involving generic “Desipramine Hydrochloride.

DateClassProductFirm
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx only, Manufactured byHeritage Pharmaceuticals Inc
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 25 mg, 100 count bottle (NDC 23155-579-01), Rx only, Manufactured by: Heritage Pharmaceuticals Inc
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 100 mg, 100 count bottle (NDC 23155-582-01), Rx only, Manufactured by:Heritage Pharmaceuticals Inc
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 150 mg, 50 count bottle (NDC 23155-583-25), Rx only, Manufactured by: Heritage Pharmaceuticals Inc
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 50 mg, 100 count bottle (NDC 23155-580-01), Rx only, Manufactured by: Heritage Pharmaceuticals Inc
2025-10-06Class IIDesipramine Hydrochloride Tablets, USP, 75 mg, 100 count bottle (NDC 23155-581-01), Rx only, Manufactured by: Heritage Pharmaceuticals Inc