Package 72162-2567-1

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 72162-2567-1
Digits Only 7216225671
Product NDC 72162-2567
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2567-1)

Marketing

Marketing Status
Marketed Since 2025-11-17
Brand citalopram
Generic citalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d3a2e1ba-b4d5-4adc-b2f7-334600c160fd", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["bef27fa1-7876-4ce3-834c-a4855aec66c9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2567-1)", "package_ndc": "72162-2567-1", "marketing_start_date": "20251117"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2567-5)", "package_ndc": "72162-2567-5", "marketing_start_date": "20251117"}], "brand_name": "Citalopram", "product_id": "72162-2567_d3a2e1ba-b4d5-4adc-b2f7-334600c160fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2567", "generic_name": "Citalopram", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}