NDC 71335-2472 – Doxepin Hydrochloride

Doxepin Hydrochloride 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2472

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 (4)

Package NDCDescriptionSince
71335-2472-160 CAPSULE in 1 BOTTLE (71335-2472-1)Nov 13, 2024
71335-2472-230 CAPSULE in 1 BOTTLE (71335-2472-2)Nov 13, 2024
71335-2472-390 CAPSULE in 1 BOTTLE (71335-2472-3)Nov 13, 2024
71335-2472-4120 CAPSULE in 1 BOTTLE (71335-2472-4)Nov 13, 2024

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