Package 72162-2227-1

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2227-1
Digits Only 7216222271
Product NDC 72162-2227
Product ID 72162-2227_28c19ac6-a51f-410e-8b88-a961ab8598a1
Description

100 CAPSULE in 1 BOTTLE (72162-2227-1)

Marketing

Marketing Status
Marketed Since 2024-01-26
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Doxepin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "28c19ac6-a51f-410e-8b88-a961ab8598a1", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000070"], "spl_set_id": ["6e22050f-95ee-410a-b770-0c32fb8b321b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2227-1)", "package_ndc": "72162-2227-1", "marketing_start_date": "20240126"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72162-2227_28c19ac6-a51f-410e-8b88-a961ab8598a1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72162-2227", "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": "25 mg/1"}], "application_number": "ANDA213474", "marketing_category": "ANDA", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}