Package 70868-810-10

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70868-810-10
Digits Only 7086881010
Product NDC 70868-810
Product ID 70868-810_241442d6-33bd-74fe-e063-6394a90a0a49
Description

100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)

Marketing

Marketing Status
Marketed Since 2022-07-18
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": "241442d6-33bd-74fe-e063-6394a90a0a49", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["9c685c94-64cd-442a-ade7-193c62d7a058"], "manufacturer_name": ["Key Therapeutics"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70868-810-10)", "package_ndc": "70868-810-10", "marketing_start_date": "20220718"}], "brand_name": "Imipramine Hydrochloride", "product_id": "70868-810_241442d6-33bd-74fe-e063-6394a90a0a49", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70868-810", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Key Therapeutics", "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": "20220718", "listing_expiration_date": "20261231"}