Package 76282-629-05

Brand: citalopram hydrobromide

Generic: citalopram
NDC Package

Package Facts

Identity

Package NDC 76282-629-05
Digits Only 7628262905
Product NDC 76282-629
Description

500 TABLET in 1 BOTTLE (76282-629-05)

Marketing

Marketing Status
Marketed Since 2017-11-10
Brand citalopram hydrobromide
Generic citalopram
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd69f24e-8108-4b9e-92ca-13ebbdf86e45", "openfda": {"upc": ["0376282208909", "0376282629902", "0376282628905"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["a8e8fde2-8392-4d5b-902b-e2b9dd55a02d"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-629-05)", "package_ndc": "76282-629-05", "marketing_start_date": "20171110"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76282-629-10)", "package_ndc": "76282-629-10", "marketing_start_date": "20171110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76282-629-30)", "package_ndc": "76282-629-30", "marketing_start_date": "20171110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-629-90)", "package_ndc": "76282-629-90", "marketing_start_date": "20171110"}], "brand_name": "CITALOPRAM HYDROBROMIDE", "product_id": "76282-629_fd69f24e-8108-4b9e-92ca-13ebbdf86e45", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "76282-629", "generic_name": "CITALOPRAM", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CITALOPRAM HYDROBROMIDE", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077534", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}