Package 70518-3767-0

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3767-0
Digits Only 7051837670
Product NDC 70518-3767
Product ID 70518-3767_3b258b90-3609-789f-e063-6394a90a9a0f
Description

30 CAPSULE in 1 BLISTER PACK (70518-3767-0)

Marketing

Marketing Status
Marketed Since 2023-06-16
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": "3b258b90-3609-789f-e063-6394a90a9a0f", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["46be666a-fb9f-42a5-a55c-ea15fd5538c9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3767-0)", "package_ndc": "70518-3767-0", "marketing_start_date": "20230616"}], "brand_name": "Doxepin hydrochloride", "product_id": "70518-3767_3b258b90-3609-789f-e063-6394a90a9a0f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3767", "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": "ANDA212624", "marketing_category": "ANDA", "marketing_start_date": "20230616", "listing_expiration_date": "20261231"}