NDC 51672-4247 – Doxepin hydrochloride

Doxepin Hydrochloride 6 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51672-4247

Product details

Brand name
Doxepin hydrochloride
Generic name
Doxepin hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA219058
Marketed since
August 7, 2025
Listing expires
December 31, 2026
Pharmacologic class
Tricyclic Antidepressant

Active ingredients

Uses, dosage, side effects and warnings for Doxepin hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51672-4247-230 TABLET in 1 BOTTLE (51672-4247-2)Aug 7, 2025

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