Package 72789-244-01

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-244-01
Digits Only 7278924401
Product NDC 72789-244
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-244-01)

Marketing

Marketing Status
Marketed Since 2022-04-14
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": "401e8e07-4fe0-1bd1-e063-6294a90ae64c", "openfda": {"upc": ["0372789243955", "0372789240954", "0372789244952"], "unii": ["BKE5Q1J60U"], "rxcui": ["835564", "835568", "835593"], "spl_set_id": ["830cb1cb-20a1-4617-a748-24241257a244"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-244-01)", "package_ndc": "72789-244-01", "marketing_start_date": "20220414"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72789-244-95)", "package_ndc": "72789-244-95", "marketing_start_date": "20221128"}], "brand_name": "Imipramine Hydrochloride", "product_id": "72789-244_401e8e07-4fe0-1bd1-e063-6294a90ae64c", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-244", "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": "50 mg/1"}], "application_number": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}