Package 69238-1057-3

Brand: desipramine hydrochloride

Generic: desipramine
NDC Package

Package Facts

Identity

Package NDC 69238-1057-3
Digits Only 6923810573
Product NDC 69238-1057
Description

30 TABLET, FILM COATED in 1 BOTTLE (69238-1057-3)

Marketing

Marketing Status
Marketed Since 2016-03-21
Brand desipramine hydrochloride
Generic desipramine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34a146f8-ed42-4e1c-9c22-6c81f6ef09f9", "openfda": {"unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["a3b4b25d-0ddb-4531-badb-f1ba3168ac07"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-1057-1)", "package_ndc": "69238-1057-1", "marketing_start_date": "20160321"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69238-1057-3)", "package_ndc": "69238-1057-3", "marketing_start_date": "20160321"}], "brand_name": "Desipramine Hydrochloride", "product_id": "69238-1057_34a146f8-ed42-4e1c-9c22-6c81f6ef09f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69238-1057", "generic_name": "Desipramine", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA208105", "marketing_category": "ANDA", "marketing_start_date": "20160321", "listing_expiration_date": "20261231"}