Package 72789-071-90

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 72789-071-90
Digits Only 7278907190
Product NDC 72789-071
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-071-90)

Marketing

Marketing Status
Marketed Since 2020-03-30
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": "47a90e31-b173-de79-e063-6394a90a05b2", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["9fe40d83-8945-4577-add5-28d52410154e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-071-30)", "package_ndc": "72789-071-30", "marketing_start_date": "20200515"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-071-90)", "package_ndc": "72789-071-90", "marketing_start_date": "20200330"}], "brand_name": "Citalopram", "product_id": "72789-071_47a90e31-b173-de79-e063-6394a90a05b2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-071", "generic_name": "Citalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20271231"}