Package 70518-4416-0

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 70518-4416-0
Digits Only 7051844160
Product NDC 70518-4416
Product ID 70518-4416_3b8bf64b-77c4-de20-e063-6394a90a4c21
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4416-0)

Marketing

Marketing Status
Marketed Since 2025-07-31
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": "3b8bf64b-77c4-de20-e063-6394a90a4c21", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["f3237467-286d-480d-8c80-b9a97738edaa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4416-0)", "package_ndc": "70518-4416-0", "marketing_start_date": "20250731"}], "brand_name": "Citalopram", "product_id": "70518-4416_3b8bf64b-77c4-de20-e063-6394a90a4c21", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4416", "generic_name": "Citalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}