Package 70518-4297-0

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4297-0
Digits Only 7051842970
Product NDC 70518-4297
Product ID 70518-4297_401df14b-32cf-1c71-e063-6394a90a6ad4
Description

30 POUCH in 1 BOX (70518-4297-0) / 1 TABLET in 1 POUCH (70518-4297-1)

Marketing

Marketing Status
Marketed Since 2025-02-27
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401df14b-32cf-1c71-e063-6394a90a6ad4", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966793"], "spl_set_id": ["7a8c56ab-5dd1-4e1a-b26a-3af45b961dd0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4297-0)  / 1 TABLET in 1 POUCH (70518-4297-1)", "package_ndc": "70518-4297-0", "marketing_start_date": "20250227"}], "brand_name": "Doxepin hydrochloride", "product_id": "70518-4297_401df14b-32cf-1c71-e063-6394a90a6ad4", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4297", "generic_name": "Doxepin hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA214823", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}