Package 72819-162-11

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 72819-162-11
Digits Only 7281916211
Product NDC 72819-162
Product ID 72819-162_0e1f91fa-a035-857e-e063-6394a90a68c9
Description

500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11)

Marketing

Marketing Status
Marketed Since 2022-02-21
Brand doxepin
Generic doxepin
Sample Package No

Linked Drug Pages (1)

Doxepin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e1f91fa-a035-857e-e063-6394a90a68c9", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["e3eac8e4-224e-4b7b-81d3-071301f914fa"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72819-162-03)", "package_ndc": "72819-162-03", "marketing_start_date": "20220221"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72819-162-10)", "package_ndc": "72819-162-10", "marketing_start_date": "20220221"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72819-162-11)", "package_ndc": "72819-162-11", "marketing_start_date": "20220221"}], "brand_name": "Doxepin", "product_id": "72819-162_0e1f91fa-a035-857e-e063-6394a90a68c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72819-162", "generic_name": "Doxepin", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA202337", "marketing_category": "ANDA", "marketing_start_date": "20210801", "listing_expiration_date": "20261231"}