NDC 23155-581 – Desipramine Hydrochloride

Desipramine Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug 6 recalls

Product NDC23155-581

Product details

Brand name
Desipramine Hydrochloride
Generic name
Desipramine hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207433
Marketed since
November 1, 2016
Marketing end
March 31, 2027
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Desipramine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
23155-581-01100 TABLET in 1 BOTTLE (23155-581-01)Nov 1, 2016

Recalls mentioning this NDC

Other Desipramine Hydrochloride products