Package 69315-135-10

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69315-135-10
Digits Only 6931513510
Product NDC 69315-135
Product ID 69315-135_2fbbe85e-9a5e-45af-bea7-e2b7ef240d3f
Description

1000 TABLET, FILM COATED in 1 BOTTLE (69315-135-10)

Marketing

Marketing Status
Marketed Since 2016-05-01
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": "2fbbe85e-9a5e-45af-bea7-e2b7ef240d3f", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564", "835568", "835593"], "spl_set_id": ["490263ce-b4d2-428a-87da-fcd07f85499a"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69315-135-01)", "package_ndc": "69315-135-01", "marketing_start_date": "20251212"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69315-135-10)", "package_ndc": "69315-135-10", "marketing_start_date": "20160501"}], "brand_name": "Imipramine Hydrochloride", "product_id": "69315-135_2fbbe85e-9a5e-45af-bea7-e2b7ef240d3f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69315-135", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}