NDC 71335-2092 – Doxepin hydrochloride

Doxepin Hydrochloride 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2092

Product details

Brand name
Doxepin hydrochloride
Generic name
Doxepin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212624
Marketed since
December 20, 2019
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
71335-2092-130 CAPSULE in 1 BOTTLE (71335-2092-1)May 17, 2022
71335-2092-260 CAPSULE in 1 BOTTLE (71335-2092-2)May 17, 2022
71335-2092-318 CAPSULE in 1 BOTTLE (71335-2092-3)May 17, 2022
71335-2092-490 CAPSULE in 1 BOTTLE (71335-2092-4)May 17, 2022
71335-2092-5180 CAPSULE in 1 BOTTLE (71335-2092-5)May 17, 2022

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