NDC 72603-222 – Doxepin

Doxepin Hydrochloride 3 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72603-222

Product details

Brand name
Doxepin
Generic name
Doxepin
Labeler
North Star Rx LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202337
Marketed since
April 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin →

Package NDC codes (1)

Package NDCDescriptionSince
72603-222-0130 TABLET, FILM COATED in 1 BOTTLE (72603-222-01)Apr 1, 2024

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