Package 50090-7819-1
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage 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
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"}