Package 42806-097-01

Brand: protriptyline hydrochloride

Generic: protriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-097-01
Digits Only 4280609701
Product NDC 42806-097
Description

100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)

Marketing

Marketing Status
Marketed Since 2013-01-09
Brand protriptyline hydrochloride
Generic protriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e68d74c7-1d6a-4453-bb46-0047047b7527", "openfda": {"upc": ["0342806097014", "0342806096307"], "unii": ["44665V00O8"], "rxcui": ["905168", "905172"], "spl_set_id": ["c6c7c39e-e510-4f4a-bf7a-926f0e075d3a"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)", "package_ndc": "42806-097-01", "marketing_start_date": "20130109"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10)", "package_ndc": "42806-097-10", "marketing_start_date": "20130109"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42806-097-30)", "package_ndc": "42806-097-30", "marketing_start_date": "20200710"}], "brand_name": "Protriptyline Hydrochloride", "product_id": "42806-097_e68d74c7-1d6a-4453-bb46-0047047b7527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "42806-097", "generic_name": "Protriptyline Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protriptyline Hydrochloride", "active_ingredients": [{"name": "PROTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202220", "marketing_category": "ANDA", "marketing_start_date": "20130109", "listing_expiration_date": "20261231"}