Package 70518-2601-3

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 70518-2601-3
Digits Only 7051826013
Product NDC 70518-2601
Product ID 70518-2601_4a69e716-1140-5ce8-e063-6394a90a57eb
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)

Marketing

Marketing Status
Marketed Since 2024-04-16
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": "4a69e716-1140-5ce8-e063-6394a90a57eb", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["aa9c1440-354f-43a6-9e70-fd7bafcb03c5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2601-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2601-2)", "package_ndc": "70518-2601-1", "marketing_start_date": "20200416"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2601-3)", "package_ndc": "70518-2601-3", "marketing_start_date": "20240416"}], "brand_name": "Citalopram", "product_id": "70518-2601_4a69e716-1140-5ce8-e063-6394a90a57eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2601", "generic_name": "citalopram", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077042", "marketing_category": "ANDA", "marketing_start_date": "20200226", "listing_expiration_date": "20271231"}