Package 72162-2517-1

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 72162-2517-1
Digits Only 7216225171
Product NDC 72162-2517
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-2517-1)

Marketing

Marketing Status
Marketed Since 2025-06-09
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "374e9dc5-bcd3-17a3-e063-6394a90af3b2", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["0bc0e09e-0f1d-4d52-b8fe-3ef8a2e5ea52"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2517-1)", "package_ndc": "72162-2517-1", "marketing_start_date": "20250609"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2517-5)", "package_ndc": "72162-2517-5", "marketing_start_date": "20250609"}], "brand_name": "Citalopram", "product_id": "72162-2517_374e9dc5-bcd3-17a3-e063-6394a90af3b2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2517", "generic_name": "Citalopram Hydrobromide", "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": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}