Package 72162-2475-3

Brand: doxepin

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2475-3
Digits Only 7216224753
Product NDC 72162-2475
Product ID 72162-2475_34297ff3-6fe5-d873-e063-6394a90a5f3e
Description

30 TABLET in 1 BOTTLE (72162-2475-3)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand doxepin
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Doxepin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34297ff3-6fe5-d873-e063-6394a90a5f3e", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966793"], "spl_set_id": ["207bb11e-6029-4506-92d2-2d8a776b9408"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2475-3)", "package_ndc": "72162-2475-3", "marketing_start_date": "20250501"}], "brand_name": "Doxepin", "product_id": "72162-2475_34297ff3-6fe5-d873-e063-6394a90a5f3e", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2475", "generic_name": "doxepin hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA202510", "marketing_category": "ANDA", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}