Package 0228-3315-03

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 0228-3315-03
Digits Only 0228331503
Product NDC 0228-3315
Product ID 0228-3315_84c77416-5f71-4fc9-b00b-964960f27241
Description

30 TABLET, FILM COATED in 1 BOTTLE (0228-3315-03)

Marketing

Marketing Status
Marketed Since 2020-01-02
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": "84c77416-5f71-4fc9-b00b-964960f27241", "openfda": {"upc": ["0302283316039"], "unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["c42333f8-1add-4f33-9458-6fe4436874a1"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0228-3315-03)", "package_ndc": "0228-3315-03", "marketing_start_date": "20200102"}], "brand_name": "Doxepin", "product_id": "0228-3315_84c77416-5f71-4fc9-b00b-964960f27241", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0228-3315", "generic_name": "Doxepin", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA201951", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}