Package 70518-4114-1

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 70518-4114-1
Digits Only 7051841141
Product NDC 70518-4114
Product ID 70518-4114_4c9aaeeb-23aa-db78-e063-6394a90ae3c4
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4114-1)

Marketing

Marketing Status
Marketed Since 2026-01-18
Brand citalopram
Generic citalopram hydrobromide
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": "4c9aaeeb-23aa-db78-e063-6394a90ae3c4", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371"], "spl_set_id": ["625a78b2-4751-4ca5-91b6-7c85fd9f8c2e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4114-1)", "package_ndc": "70518-4114-1", "marketing_start_date": "20260118"}], "brand_name": "Citalopram", "product_id": "70518-4114_4c9aaeeb-23aa-db78-e063-6394a90ae3c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4114", "generic_name": "Citalopram Hydrobromide", "labeler_name": "REMEDYREPACK INC.", "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": "20240626", "listing_expiration_date": "20271231"}