Package 67046-1564-3

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1564-3
Digits Only 6704615643
Product NDC 67046-1564
Product ID 67046-1564_48e8b30a-0294-a5ed-e063-6394a90a8f01
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1564-3)

Marketing

Marketing Status
Marketed Since 2026-01-21
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": "48e8b30a-0294-a5ed-e063-6394a90a8f01", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["48e8b819-a9a0-aa5a-e063-6394a90ad9c2"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1564-3)", "package_ndc": "67046-1564-3", "marketing_start_date": "20260121"}], "brand_name": "Imipramine Hydrochloride", "product_id": "67046-1564_48e8b30a-0294-a5ed-e063-6394a90a8f01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "67046-1564", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20260121", "listing_expiration_date": "20271231"}