Package 70518-1588-0

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1588-0
Digits Only 7051815880
Product NDC 70518-1588
Product ID 70518-1588_494e4586-13e0-bc7a-e063-6294a90a90cb
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)

Marketing

Marketing Status
Marketed Since 2018-10-25
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": "494e4586-13e0-bc7a-e063-6294a90a90cb", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835568"], "spl_set_id": ["db007ac0-020e-4962-8903-7497ab96a74e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)", "package_ndc": "70518-1588-0", "marketing_start_date": "20181025"}], "brand_name": "Imipramine Hydrochloride", "product_id": "70518-1588_494e4586-13e0-bc7a-e063-6294a90a90cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-1588", "generic_name": "Imipramine Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20181025", "listing_expiration_date": "20271231"}