Package 43063-481-05

Brand: citalopram

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 43063-481-05
Digits Only 4306348105
Product NDC 43063-481
Description

5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05)

Marketing

Marketing Status
Marketed Since 2015-04-03
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": "2f361594-eb68-f951-e063-6294a90a5006", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["283672"], "spl_set_id": ["df929b3f-0cda-4a75-96d3-22e6b0edbbc9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-05)", "package_ndc": "43063-481-05", "marketing_start_date": "20150403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-481-30)", "package_ndc": "43063-481-30", "marketing_start_date": "20161027"}], "brand_name": "Citalopram", "product_id": "43063-481_2f361594-eb68-f951-e063-6294a90a5006", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43063-481", "generic_name": "Citalopram", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20071018", "listing_expiration_date": "20261231"}