Package 72162-2228-1
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
72162-2228-1
Digits Only
7216222281
Product NDC
72162-2228
Description
100 CAPSULE in 1 BOTTLE (72162-2228-1)
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": "aed9708c-54a5-4b76-b137-4cfcb47e89c9", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000097"], "spl_set_id": ["a4c804e3-4706-48d8-b928-b22c2dcaeed8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2228-1)", "package_ndc": "72162-2228-1", "marketing_start_date": "20240126"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72162-2228_aed9708c-54a5-4b76-b137-4cfcb47e89c9", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2228", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA213474", "marketing_category": "ANDA", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}