Package 68999-540-24

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 68999-540-24
Digits Only 6899954024
Product NDC 68999-540
Description

2 TRAY in 1 BOX (68999-540-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)

Marketing

Marketing Status
Marketed Since 2026-01-13
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": "484c3f19-d5f7-3e00-e063-6394a90a1938", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["3114274f-d81f-4b1f-8f17-35db9eee2ffe"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-540-24)  / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-540-10)", "package_ndc": "68999-540-24", "marketing_start_date": "20260113"}], "brand_name": "Citalopram", "product_id": "68999-540_484c3f19-d5f7-3e00-e063-6394a90a1938", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68999-540", "generic_name": "Citalopram", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077629", "marketing_category": "ANDA", "marketing_start_date": "20060614", "listing_expiration_date": "20271231"}