Package 70518-4327-0

Brand: doxepin

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4327-0
Digits Only 7051843270
Product NDC 70518-4327
Product ID 70518-4327_4265ca2a-3730-e458-e063-6294a90a1973
Description

30 POUCH in 1 BOX (70518-4327-0) / 1 TABLET in 1 POUCH (70518-4327-1)

Marketing

Marketing Status
Marketed Since 2025-04-13
Brand doxepin
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": "4265ca2a-3730-e458-e063-6294a90a1973", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966793"], "spl_set_id": ["2a9c2159-e89e-47e4-b91c-ac5560607a2d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4327-0)  / 1 TABLET in 1 POUCH (70518-4327-1)", "package_ndc": "70518-4327-0", "marketing_start_date": "20250413"}], "brand_name": "Doxepin", "product_id": "70518-4327_4265ca2a-3730-e458-e063-6294a90a1973", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4327", "generic_name": "doxepin hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20250413", "listing_expiration_date": "20261231"}