Package 68071-3558-1

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 68071-3558-1
Digits Only 6807135581
Product NDC 68071-3558
Product ID 68071-3558_0dfb11d9-f48e-56ee-e063-6294a90ad256
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)

Marketing

Marketing Status
Marketed Since 2024-01-02
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": "0dfb11d9-f48e-56ee-e063-6294a90ad256", "openfda": {"upc": ["0368071355819"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["0dfb11d9-f48d-56ee-e063-6294a90ad256"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3558-1)", "package_ndc": "68071-3558-1", "marketing_start_date": "20240102"}], "brand_name": "Citalopram", "product_id": "68071-3558_0dfb11d9-f48e-56ee-e063-6294a90ad256", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-3558", "generic_name": "citalopram", "labeler_name": "NuCare Pharmaceuticals,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": "20080728", "listing_expiration_date": "20261231"}