Package 50090-3148-0

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3148-0
Digits Only 5009031480
Product NDC 50090-3148
Product ID 50090-3148_628d179c-a31b-4886-9f57-cb2c3fb32efd
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-3148-0)

Marketing

Marketing Status
Marketed Since 2017-10-03
Brand imipramine hydrochloride
Generic imipramine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "628d179c-a31b-4886-9f57-cb2c3fb32efd", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["d9dbcebe-9aba-4a93-a7b7-48d29e07d3c4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3148-0)", "package_ndc": "50090-3148-0", "marketing_start_date": "20171003"}], "brand_name": "Imipramine Hydrochloride", "product_id": "50090-3148_628d179c-a31b-4886-9f57-cb2c3fb32efd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-3148", "generic_name": "Imipramine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20160407", "listing_expiration_date": "20261231"}