Package 72789-493-95
Brand: imipramine hydrochloride
Generic: imipramine hydrochloridePackage Facts
Identity
Package NDC
72789-493-95
Digits Only
7278949395
Product NDC
72789-493
Description
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-493-95)
Marketing
Marketing Status
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": "43f45733-f09e-ff01-e063-6294a90a07ad", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835568"], "spl_set_id": ["7091ff32-55b9-48fd-a86d-c502af57473f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-493-01)", "package_ndc": "72789-493-01", "marketing_start_date": "20250903"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-493-95)", "package_ndc": "72789-493-95", "marketing_start_date": "20250310"}], "brand_name": "Imipramine Hydrochloride", "product_id": "72789-493_43f45733-f09e-ff01-e063-6294a90a07ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-493", "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": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}