Package 0054-0062-58

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 0054-0062-58
Digits Only 0054006258
Product NDC 0054-0062
Product ID 0054-0062_6a701183-6c4f-448f-a05a-81ee7f5b734f
Description

1 BOTTLE, PLASTIC in 1 CARTON (0054-0062-58) / 240 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2004-05-25
Brand citalopram
Generic citalopram
Sample Package No

Linked Drug Pages (1)

Citalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6a701183-6c4f-448f-a05a-81ee7f5b734f", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["29408d84-7b00-4cee-969c-8095f8083ff5"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0054-0062-58)  / 240 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0054-0062-58", "marketing_start_date": "20040525"}], "brand_name": "Citalopram", "product_id": "0054-0062_6a701183-6c4f-448f-a05a-81ee7f5b734f", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0054-0062", "generic_name": "Citalopram", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077043", "marketing_category": "ANDA", "marketing_start_date": "20040525", "listing_expiration_date": "20261231"}