Package 68645-559-54

Brand: citalopram hydrobromide

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 68645-559-54
Digits Only 6864555954
Product NDC 68645-559
Product ID 68645-559_2c503073-e1f5-5911-e063-6394a90adfd2
Description

30 TABLET in 1 BOTTLE (68645-559-54)

Marketing

Marketing Status
Marketed Since 2007-10-18
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": "2c503073-e1f5-5911-e063-6394a90adfd2", "openfda": {"upc": ["0368645559544"], "unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["719276c0-ec1f-4bb4-9cea-e104202689c9"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-559-54)", "package_ndc": "68645-559-54", "marketing_start_date": "20071018"}], "brand_name": "Citalopram Hydrobromide", "product_id": "68645-559_2c503073-e1f5-5911-e063-6394a90adfd2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68645-559", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram Hydrobromide", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078216", "marketing_category": "ANDA", "marketing_start_date": "20071018", "listing_expiration_date": "20261231"}