Package 80425-0342-2

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0342-2
Digits Only 8042503422
Product NDC 80425-0342
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0342-2)

Marketing

Marketing Status
Marketed Since 2023-06-06
Brand imipramine hydrochloride
Generic imipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9c2eb6-a6db-f647-e063-6294a90a93fe", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["fd78fb8e-99ae-91b0-e053-6394a90a9271"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0342-1)", "package_ndc": "80425-0342-1", "marketing_start_date": "20230606"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0342-2)", "package_ndc": "80425-0342-2", "marketing_start_date": "20230606"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0342-3)", "package_ndc": "80425-0342-3", "marketing_start_date": "20230606"}], "brand_name": "Imipramine Hydrochloride", "product_id": "80425-0342_2a9c2eb6-a6db-f647-e063-6294a90a93fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "80425-0342", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20230606", "listing_expiration_date": "20261231"}