NDC 71335-2804 – Doxepin Hydrochloride

Doxepin Hydrochloride 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2804

Product details

Brand name
Doxepin Hydrochloride
Generic name
Doxepin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215113
Marketed since
June 27, 2022
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
71335-2804-160 CAPSULE in 1 BOTTLE, PLASTIC (71335-2804-1)Oct 13, 2025
71335-2804-230 CAPSULE in 1 BOTTLE, PLASTIC (71335-2804-2)Oct 13, 2025
71335-2804-390 CAPSULE in 1 BOTTLE, PLASTIC (71335-2804-3)Oct 13, 2025
71335-2804-4120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2804-4)Oct 13, 2025

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