NDC 71335-2647 – Doxepin Hydrochloride

Doxepin Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2647

Product details

Brand name
Doxepin Hydrochloride
Generic name
Doxepin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215076
Marketed since
April 23, 2021
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
71335-2647-130 CAPSULE in 1 BOTTLE (71335-2647-1)Jun 3, 2025
71335-2647-260 CAPSULE in 1 BOTTLE (71335-2647-2)Jun 3, 2025
71335-2647-318 CAPSULE in 1 BOTTLE (71335-2647-3)Jun 3, 2025
71335-2647-490 CAPSULE in 1 BOTTLE (71335-2647-4)Jun 3, 2025
71335-2647-5180 CAPSULE in 1 BOTTLE (71335-2647-5)Jun 3, 2025

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