Package 70518-4334-0

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 70518-4334-0
Digits Only 7051843340
Product NDC 70518-4334
Product ID 70518-4334_3401590f-c858-2164-e063-6294a90a7ea1
Description

100 POUCH in 1 BOX (70518-4334-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4334-1)

Marketing

Marketing Status
Marketed Since 2025-04-28
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": "3401590f-c858-2164-e063-6294a90a7ea1", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["0109f365-bebd-4810-a56f-4451e10245db"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4334-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4334-1)", "package_ndc": "70518-4334-0", "marketing_start_date": "20250428"}], "brand_name": "Citalopram", "product_id": "70518-4334_3401590f-c858-2164-e063-6294a90a7ea1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4334", "generic_name": "Citalopram Hydrobromide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20250428", "listing_expiration_date": "20261231"}