Package 70518-4282-0

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4282-0
Digits Only 7051842820
Product NDC 70518-4282
Product ID 70518-4282_4019f5bb-f9ab-92fc-e063-6394a90aa042
Description

30 CAPSULE in 1 BLISTER PACK (70518-4282-0)

Marketing

Marketing Status
Marketed Since 2025-02-10
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": "4019f5bb-f9ab-92fc-e063-6394a90aa042", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["21dc77be-23af-4a1f-b189-dfee8ae2f894"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4282-0)", "package_ndc": "70518-4282-0", "marketing_start_date": "20250210"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "70518-4282_4019f5bb-f9ab-92fc-e063-6394a90aa042", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4282", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}