Package 82804-957-72
Brand: imipramine hydrochloride
Generic: imipramine hydrochloridePackage Facts
Identity
Package NDC
82804-957-72
Digits Only
8280495772
Product NDC
82804-957
Description
120 TABLET in 1 BOTTLE (82804-957-72)
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": "5997822f-ce83-4091-be71-21a6b01caaba", "openfda": {"upc": ["0382804957309", "0382804956302", "0382804958306"], "unii": ["BKE5Q1J60U"], "rxcui": ["835564", "835568", "835593"], "spl_set_id": ["5997822f-ce83-4091-be71-21a6b01caaba"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-957-00)", "package_ndc": "82804-957-00", "marketing_start_date": "20260112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-957-11)", "package_ndc": "82804-957-11", "marketing_start_date": "20260112"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-957-30)", "package_ndc": "82804-957-30", "marketing_start_date": "20260112"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-957-55)", "package_ndc": "82804-957-55", "marketing_start_date": "20260112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-957-60)", "package_ndc": "82804-957-60", "marketing_start_date": "20260112"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-957-72)", "package_ndc": "82804-957-72", "marketing_start_date": "20260112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-957-90)", "package_ndc": "82804-957-90", "marketing_start_date": "20260112"}], "brand_name": "Imipramine Hydrochloride", "product_id": "82804-957_5997822f-ce83-4091-be71-21a6b01caaba", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-957", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}