Package 69584-426-90

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69584-426-90
Digits Only 6958442690
Product NDC 69584-426
Product ID 69584-426_1509ebac-0e7d-4b02-ba2e-bf188a26fd77
Description

1000 TABLET in 1 BOTTLE (69584-426-90)

Marketing

Marketing Status
Marketed Since 2022-05-15
Brand imipramine hydrochloride
Generic imipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Imipramine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1509ebac-0e7d-4b02-ba2e-bf188a26fd77", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564", "835568", "835593"], "spl_set_id": ["a5f60cf1-6f14-40a3-a794-9d69b28088d8"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-426-10)", "package_ndc": "69584-426-10", "marketing_start_date": "20200801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69584-426-90)", "package_ndc": "69584-426-90", "marketing_start_date": "20220515"}], "brand_name": "Imipramine Hydrochloride", "product_id": "69584-426_1509ebac-0e7d-4b02-ba2e-bf188a26fd77", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69584-426", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Oxford Pharmaceuticals, 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": "20200801", "listing_expiration_date": "20271231"}