Doxepin Hydrochloride 51672-4247-02

Package NDC

51672-4247-02

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 7, 2025
Listing Expires: December 31, 2026
Application: ANDA219058

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Active Ingredients

Ingredient	Strength
Doxepin Hydrochloride	6 mg/1

Drug Class

Tricyclic Antidepressant [EPC]

Selected Package

51672-4247-02Selected

30 TABLET in 1 BOTTLE (51672-4247-2)