NDC 71335-0072 – Doxepin Hydrochloride

Doxepin Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0072

Product details

Brand name
Doxepin Hydrochloride
Generic name
Doxepin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207482
Marketed since
June 28, 2017
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-0072-130 CAPSULE in 1 BOTTLE (71335-0072-1)Jan 22, 2020
71335-0072-260 CAPSULE in 1 BOTTLE (71335-0072-2)Jan 28, 2025
71335-0072-318 CAPSULE in 1 BOTTLE (71335-0072-3)Jan 28, 2025
71335-0072-490 CAPSULE in 1 BOTTLE (71335-0072-4)Jan 28, 2025
71335-0072-5180 CAPSULE in 1 BOTTLE (71335-0072-5)Jan 28, 2025

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