Package 70518-4238-0

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4238-0
Digits Only 7051842380
Product NDC 70518-4238
Product ID 70518-4238_4006d7dd-8a75-241d-e063-6394a90adde1
Description

30 CAPSULE in 1 BLISTER PACK (70518-4238-0)

Marketing

Marketing Status
Marketed Since 2024-12-13
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Doxepin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4006d7dd-8a75-241d-e063-6394a90adde1", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000070"], "spl_set_id": ["d29a8c70-cf1c-4bf8-bb87-1c80babce64e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4238-0)", "package_ndc": "70518-4238-0", "marketing_start_date": "20241213"}], "brand_name": "Doxepin Hydrochloride", "product_id": "70518-4238_4006d7dd-8a75-241d-e063-6394a90adde1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4238", "generic_name": "Doxepin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA215113", "marketing_category": "ANDA", "marketing_start_date": "20241213", "listing_expiration_date": "20261231"}