NDC 10135-758 – Doxepin

Doxepin Hydrochloride 3 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC10135-758

Product details

Brand name
Doxepin
Generic name
Doxepin
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202337
Marketed since
October 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin →

Package NDC codes (1)

Package NDCDescriptionSince
10135-758-3030 TABLET, FILM COATED in 1 BOTTLE (10135-758-30)Oct 1, 2023

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