Package 65862-007-30

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 65862-007-30
Digits Only 6586200730
Product NDC 65862-007
Description

30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)

Marketing

Marketing Status
Marketed Since 2004-10-28
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5642ea11-17b4-431a-a896-2cb336929100", "openfda": {"upc": ["0365862007308", "0365862006301", "0365862005304"], "unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["2632b547-2e13-447f-ac85-c774e437d6a8"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)", "package_ndc": "65862-007-01", "marketing_start_date": "20041028"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-007-05)", "package_ndc": "65862-007-05", "marketing_start_date": "20041028"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-007-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-007-10", "marketing_start_date": "20041028"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-007-30)", "package_ndc": "65862-007-30", "marketing_start_date": "20041028"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (65862-007-32)", "package_ndc": "65862-007-32", "marketing_start_date": "20041028"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (65862-007-60)", "package_ndc": "65862-007-60", "marketing_start_date": "20041028"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-007-90)", "package_ndc": "65862-007-90", "marketing_start_date": "20041028"}], "brand_name": "Citalopram", "product_id": "65862-007_5642ea11-17b4-431a-a896-2cb336929100", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-007", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}