Package 72789-492-01

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-492-01
Digits Only 7278949201
Product NDC 72789-492
Product ID 72789-492_43f44b1e-5aaa-0f6d-e063-6394a90a5add
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-01)

Marketing

Marketing Status
Marketed Since 2025-09-03
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": "43f44b1e-5aaa-0f6d-e063-6394a90a5add", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["649837df-147f-436c-9553-32ffecf4c6f1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-01)", "package_ndc": "72789-492-01", "marketing_start_date": "20250903"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-492-95)", "package_ndc": "72789-492-95", "marketing_start_date": "20250310"}], "brand_name": "Imipramine Hydrochloride", "product_id": "72789-492_43f44b1e-5aaa-0f6d-e063-6394a90a5add", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-492", "generic_name": "Imipramine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}