NDC 72819-162 – Doxepin

Doxepin Hydrochloride 6 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72819-162

Product details

Brand name
Doxepin
Generic name
Doxepin
Labeler
Archis Pharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202337
Marketed since
August 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin →

Package NDC codes (3)

Package NDCDescriptionSince
72819-162-0330 TABLET, FILM COATED in 1 BOTTLE (72819-162-03)Feb 21, 2022
72819-162-10100 TABLET, FILM COATED in 1 BOTTLE (72819-162-10)Feb 21, 2022
72819-162-11500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11)Feb 21, 2022

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