Package 65862-074-24

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 65862-074-24
Digits Only 6586207424
Product NDC 65862-074
Product ID 65862-074_7cecadcf-9da0-41e4-b9fd-0fe04572dcd8
Description

240 mL in 1 BOTTLE (65862-074-24)

Marketing

Marketing Status
Marketed Since 2006-08-28
Brand citalopram hydrobromide
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram Hydrobromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7cecadcf-9da0-41e4-b9fd-0fe04572dcd8", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309313"], "spl_set_id": ["e7a2cbdd-1bdb-4e59-a3dd-298a189753ae"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (65862-074-24)", "package_ndc": "65862-074-24", "marketing_start_date": "20060828"}], "brand_name": "Citalopram Hydrobromide", "product_id": "65862-074_7cecadcf-9da0-41e4-b9fd-0fe04572dcd8", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65862-074", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA077812", "marketing_category": "ANDA", "marketing_start_date": "20060828", "listing_expiration_date": "20261231"}