Package 72162-2226-0

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2226-0
Digits Only 7216222260
Product NDC 72162-2226
Description

1000 CAPSULE in 1 BOTTLE (72162-2226-0)

Marketing

Marketing Status
Marketed Since 2024-01-26
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": "840ddc4a-3c80-4833-aa84-96702e152d9d", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000058"], "spl_set_id": ["874ac945-e4b0-4b0a-8938-904b3b66d8c6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72162-2226-0)", "package_ndc": "72162-2226-0", "marketing_start_date": "20240126"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2226-1)", "package_ndc": "72162-2226-1", "marketing_start_date": "20240126"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72162-2226_840ddc4a-3c80-4833-aa84-96702e152d9d", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2226", "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": "100 mg/1"}], "application_number": "ANDA215483", "marketing_category": "ANDA", "marketing_start_date": "20211201", "listing_expiration_date": "20261231"}