Package 0456-4040-01

Brand: celexa

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 0456-4040-01
Digits Only 0456404001
Product NDC 0456-4040
Product ID 0456-4040_0eee9751-8886-474c-a806-8003e90cb151
Description

100 TABLET, FILM COATED in 1 BOTTLE (0456-4040-01)

Marketing

Marketing Status
Marketed Since 1998-07-17
Brand celexa
Generic citalopram
Sample Package No

Linked Drug Pages (1)

Celexa ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0eee9751-8886-474c-a806-8003e90cb151", "openfda": {"upc": ["0304564010018", "0304564020017", "0304564040015"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "213344", "213345", "283672", "284591", "309314"], "spl_set_id": ["4259d9b1-de34-43a4-85a8-41dd214e9177"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0456-4040-01)", "package_ndc": "0456-4040-01", "marketing_start_date": "19980717"}], "brand_name": "Celexa", "product_id": "0456-4040_0eee9751-8886-474c-a806-8003e90cb151", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0456-4040", "generic_name": "citalopram", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Celexa", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "NDA020822", "marketing_category": "NDA", "marketing_start_date": "19980717", "listing_expiration_date": "20261231"}