Package 50090-7819-1

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7819-1
Digits Only 5009078191
Product NDC 50090-7819
Description

30 CAPSULE in 1 BOTTLE (50090-7819-1)

Marketing

Marketing Status
Marketed Since 2025-12-11
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "51e41985-0be0-4965-8562-d1df183e2575", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["e0460c02-3dae-4b19-845c-2ffcfb587f6d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7819-1)", "package_ndc": "50090-7819-1", "marketing_start_date": "20251211"}], "brand_name": "Doxepin Hydrochloride", "product_id": "50090-7819_51e41985-0be0-4965-8562-d1df183e2575", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-7819", "generic_name": "Doxepin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA215113", "marketing_category": "ANDA", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}