Package 71610-413-60

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 71610-413-60
Digits Only 7161041360
Product NDC 71610-413
Product ID 71610-413_fc10ffe3-e320-4a92-9b34-1f56d369691b
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-413-60)

Marketing

Marketing Status
Marketed Since 2020-04-03
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc10ffe3-e320-4a92-9b34-1f56d369691b", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["309314"], "spl_set_id": ["31ddd184-7560-473c-b674-5fa3187c5598"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-413-60)", "package_ndc": "71610-413-60", "marketing_start_date": "20200403"}], "brand_name": "Citalopram", "product_id": "71610-413_fc10ffe3-e320-4a92-9b34-1f56d369691b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-413", "generic_name": "Citalopram Hydrobromide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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"}