Package 45963-345-02

Brand: desipramine hydrochloride

Generic: desipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45963-345-02
Digits Only 4596334502
Product NDC 45963-345
Description

100 TABLET, FILM COATED in 1 BOTTLE (45963-345-02)

Marketing

Marketing Status
Marketed Since 2006-07-19
Brand desipramine hydrochloride
Generic desipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb512a98-31c9-4ae9-9cc9-1d102302cfea", "openfda": {"upc": ["0345963345028", "0345963346506", "0345963344021", "0345963343024", "0345963341020"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["ba02a95d-d82e-4a13-90b4-a219abc0249a"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (45963-345-02)", "package_ndc": "45963-345-02", "marketing_start_date": "20060719"}], "brand_name": "Desipramine Hydrochloride", "product_id": "45963-345_cb512a98-31c9-4ae9-9cc9-1d102302cfea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "45963-345", "generic_name": "Desipramine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA071766", "marketing_category": "ANDA", "marketing_start_date": "20060719", "listing_expiration_date": "20261231"}