Package 55154-3329-0
Brand: citalopram
Generic: citalopramPackage Facts
Identity
Package NDC
55154-3329-0
Digits Only
5515433290
Product NDC
55154-3329
Description
10 BLISTER PACK in 1 BAG (55154-3329-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
citalopram
Generic
citalopram
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "194b0b9f-45cf-4b49-a13e-e05257f05ab4", "openfda": {"upc": ["0055154332903", "0055154334907"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["6c8942f8-963a-4007-a147-b77ac629e4d4"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3329-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-3329-0", "marketing_start_date": "20091102"}], "brand_name": "Citalopram", "product_id": "55154-3329_194b0b9f-45cf-4b49-a13e-e05257f05ab4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-3329", "generic_name": "Citalopram", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20091102", "listing_expiration_date": "20261231"}