NDC 71335-2188 – Doxepin hydrochloride

Doxepin Hydrochloride 25 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2188

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
71335-2188-130 CAPSULE in 1 BOTTLE (71335-2188-1)Nov 15, 2022
71335-2188-260 CAPSULE in 1 BOTTLE (71335-2188-2)Nov 15, 2022
71335-2188-328 CAPSULE in 1 BOTTLE (71335-2188-3)Nov 15, 2022
71335-2188-418 CAPSULE in 1 BOTTLE (71335-2188-4)Nov 15, 2022
71335-2188-590 CAPSULE in 1 BOTTLE (71335-2188-5)Nov 15, 2022

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