Package 70518-2553-1

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 70518-2553-1
Digits Only 7051825531
Product NDC 70518-2553
Product ID 70518-2553_4a67aedb-35d4-e009-e063-6394a90a467c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2553-1)

Marketing

Marketing Status
Marketed Since 2025-01-30
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": "4a67aedb-35d4-e009-e063-6394a90a467c", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["f79f878e-99fb-4757-8abb-931af1fa9e2b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2553-1)", "package_ndc": "70518-2553-1", "marketing_start_date": "20250130"}], "brand_name": "Citalopram", "product_id": "70518-2553_4a67aedb-35d4-e009-e063-6394a90a467c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2553", "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": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20200122", "listing_expiration_date": "20271231"}