Package 70518-3526-0

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3526-0
Digits Only 7051835260
Product NDC 70518-3526
Product ID 70518-3526_3f14b9c9-5d0e-d2ec-e063-6294a90a6815
Description

30 TABLET in 1 BLISTER PACK (70518-3526-0)

Marketing

Marketing Status
Marketed Since 2020-09-19
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": "3f14b9c9-5d0e-d2ec-e063-6294a90a6815", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["02c19a0a-3d9d-4881-ad14-1687aafd87b5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3526-0)", "package_ndc": "70518-3526-0", "marketing_start_date": "20200919"}], "brand_name": "Imipramine Hydrochloride", "product_id": "70518-3526_3f14b9c9-5d0e-d2ec-e063-6294a90a6815", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3526", "generic_name": "Imipramine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20200919", "listing_expiration_date": "20261231"}