Package 72603-223-01

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 72603-223-01
Digits Only 7260322301
Product NDC 72603-223
Product ID 72603-223_472f1364-17cc-0996-e063-6394a90aa786
Description

30 TABLET, FILM COATED in 1 BOTTLE (72603-223-01)

Marketing

Marketing Status
Marketed Since 2024-04-01
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": "472f1364-17cc-0996-e063-6394a90aa786", "openfda": {"upc": ["0372603222012", "0372603223019"], "unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["12edd5c6-c863-b83a-e063-6294a90a2f36"], "manufacturer_name": ["North Star Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72603-223-01)", "package_ndc": "72603-223-01", "marketing_start_date": "20240401"}], "brand_name": "Doxepin", "product_id": "72603-223_472f1364-17cc-0996-e063-6394a90aa786", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72603-223", "generic_name": "Doxepin", "labeler_name": "North Star Rx 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": "20240401", "listing_expiration_date": "20261231"}