Package 0904-6084-61

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 0904-6084-61
Digits Only 0904608461
Product NDC 0904-6084
Product ID 0904-6084_5bf8d853-5669-4ef2-940e-6c9075a45ce9
Description

100 BLISTER PACK in 1 CARTON (0904-6084-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-11-02
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": "5bf8d853-5669-4ef2-940e-6c9075a45ce9", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672"], "spl_set_id": ["a6949652-b15b-435b-9097-2219f398ac05"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6084-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6084-61", "marketing_start_date": "20091102"}], "brand_name": "Citalopram", "product_id": "0904-6084_5bf8d853-5669-4ef2-940e-6c9075a45ce9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0904-6084", "generic_name": "Citalopram", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20091102", "listing_expiration_date": "20271231"}